Corrigendum to

Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease (Am J Med Genet A., (2016), 170A, 10, 2719-2730, 10.1002/ajmg.a.37817)

Prajnya Ranganath, Divya Matta, Gandham Sri Lakshmi Bhavani, Savita Wangnekar, Jamal Mohammed Nurul Jain, Ishwar C. Verma, Madhulika Kabra, Ratna D. Puri, Sumita Danda, Neerja Gupta, Katta M. Girisha, Vaikom H. Sankar, Siddaramappa J. Patil, Akella Radha Rama Devi, Meenakshi Bhat, Kalpana Gowrishankar, Kausik Mandal, Shagun Aggarwal, Parag Mohan Tamhankar, Preetha Tilak & 2 others Shubha R. Phadke, Ashwin Dalal

Research output: Contribution to journalComment/debate

1 Citation (Scopus)

Abstract

Authors Ashwin Dalal This article corrects: Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease, Am J Med Genet A. 2016 Oct; Volume 170A, Issue 10, 2719–2730, Article first published online: June 24 2016. There was an error in the mutation description of the patient number 59 in Table I reported in this article. The correct mutation description in this patient with Niemann Pick disease Type A is NG_011780.1: g.8462_8560dup (and not NG_011780.1:g.3471_3570dup). Dr. Andrew Phillips, Research Associate, Human Gene Mutation Database, UK detected this mistake when reviewing the mutations in patients with this disease for the database. I am grateful that he informed us about this, and that this can be corrected now.

Original languageEnglish
Number of pages1
JournalAmerican Journal of Medical Genetics, Part A
Volume173
Issue number3
DOIs
Publication statusPublished - 01-03-2017

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Viverridae
Sphingomyelin Phosphodiesterase
Mutation
Acids
Genes
Type A Niemann-Pick Disease
Databases
corrigendum
Research

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

Cite this

Ranganath, Prajnya ; Matta, Divya ; Bhavani, Gandham Sri Lakshmi ; Wangnekar, Savita ; Jain, Jamal Mohammed Nurul ; Verma, Ishwar C. ; Kabra, Madhulika ; Puri, Ratna D. ; Danda, Sumita ; Gupta, Neerja ; Girisha, Katta M. ; Sankar, Vaikom H. ; Patil, Siddaramappa J. ; Devi, Akella Radha Rama ; Bhat, Meenakshi ; Gowrishankar, Kalpana ; Mandal, Kausik ; Aggarwal, Shagun ; Tamhankar, Parag Mohan ; Tilak, Preetha ; Phadke, Shubha R. ; Dalal, Ashwin. / Corrigendum to : Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease (Am J Med Genet A., (2016), 170A, 10, 2719-2730, 10.1002/ajmg.a.37817). In: American Journal of Medical Genetics, Part A. 2017 ; Vol. 173, No. 3.
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title = "Corrigendum to: Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease (Am J Med Genet A., (2016), 170A, 10, 2719-2730, 10.1002/ajmg.a.37817)",
abstract = "Authors Ashwin Dalal This article corrects: Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease, Am J Med Genet A. 2016 Oct; Volume 170A, Issue 10, 2719–2730, Article first published online: June 24 2016. There was an error in the mutation description of the patient number 59 in Table I reported in this article. The correct mutation description in this patient with Niemann Pick disease Type A is NG_011780.1: g.8462_8560dup (and not NG_011780.1:g.3471_3570dup). Dr. Andrew Phillips, Research Associate, Human Gene Mutation Database, UK detected this mistake when reviewing the mutations in patients with this disease for the database. I am grateful that he informed us about this, and that this can be corrected now.",
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Ranganath, P, Matta, D, Bhavani, GSL, Wangnekar, S, Jain, JMN, Verma, IC, Kabra, M, Puri, RD, Danda, S, Gupta, N, Girisha, KM, Sankar, VH, Patil, SJ, Devi, ARR, Bhat, M, Gowrishankar, K, Mandal, K, Aggarwal, S, Tamhankar, PM, Tilak, P, Phadke, SR & Dalal, A 2017, 'Corrigendum to: Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease (Am J Med Genet A., (2016), 170A, 10, 2719-2730, 10.1002/ajmg.a.37817)', American Journal of Medical Genetics, Part A, vol. 173, no. 3. https://doi.org/10.1002/ajmg.a.38040

Corrigendum to : Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease (Am J Med Genet A., (2016), 170A, 10, 2719-2730, 10.1002/ajmg.a.37817). / Ranganath, Prajnya; Matta, Divya; Bhavani, Gandham Sri Lakshmi; Wangnekar, Savita; Jain, Jamal Mohammed Nurul; Verma, Ishwar C.; Kabra, Madhulika; Puri, Ratna D.; Danda, Sumita; Gupta, Neerja; Girisha, Katta M.; Sankar, Vaikom H.; Patil, Siddaramappa J.; Devi, Akella Radha Rama; Bhat, Meenakshi; Gowrishankar, Kalpana; Mandal, Kausik; Aggarwal, Shagun; Tamhankar, Parag Mohan; Tilak, Preetha; Phadke, Shubha R.; Dalal, Ashwin.

In: American Journal of Medical Genetics, Part A, Vol. 173, No. 3, 01.03.2017.

Research output: Contribution to journalComment/debate

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AU - Ranganath, Prajnya

AU - Matta, Divya

AU - Bhavani, Gandham Sri Lakshmi

AU - Wangnekar, Savita

AU - Jain, Jamal Mohammed Nurul

AU - Verma, Ishwar C.

AU - Kabra, Madhulika

AU - Puri, Ratna D.

AU - Danda, Sumita

AU - Gupta, Neerja

AU - Girisha, Katta M.

AU - Sankar, Vaikom H.

AU - Patil, Siddaramappa J.

AU - Devi, Akella Radha Rama

AU - Bhat, Meenakshi

AU - Gowrishankar, Kalpana

AU - Mandal, Kausik

AU - Aggarwal, Shagun

AU - Tamhankar, Parag Mohan

AU - Tilak, Preetha

AU - Phadke, Shubha R.

AU - Dalal, Ashwin

PY - 2017/3/1

Y1 - 2017/3/1

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AB - Authors Ashwin Dalal This article corrects: Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease, Am J Med Genet A. 2016 Oct; Volume 170A, Issue 10, 2719–2730, Article first published online: June 24 2016. There was an error in the mutation description of the patient number 59 in Table I reported in this article. The correct mutation description in this patient with Niemann Pick disease Type A is NG_011780.1: g.8462_8560dup (and not NG_011780.1:g.3471_3570dup). Dr. Andrew Phillips, Research Associate, Human Gene Mutation Database, UK detected this mistake when reviewing the mutations in patients with this disease for the database. I am grateful that he informed us about this, and that this can be corrected now.

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JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

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