A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy

Anju Shukla, Dhanya L. Narayanan, Urja Asher, Katta M. Girisha

Research output: Contribution to journalLetter

Original languageEnglish
Pages (from-to)276-277
Number of pages2
JournalClinical Genetics
Volume96
Issue number3
DOIs
Publication statusPublished - 01-01-2019

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

Cite this

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title = "A novel bi-allelic loss-of-function variant in MYOD1: Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy",
author = "Anju Shukla and Narayanan, {Dhanya L.} and Urja Asher and Girisha, {Katta M.}",
year = "2019",
month = "1",
day = "1",
doi = "10.1111/cge.13596",
language = "English",
volume = "96",
pages = "276--277",
journal = "Clinical Genetics",
issn = "0009-9163",
publisher = "Wiley-Blackwell",
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}

A novel bi-allelic loss-of-function variant in MYOD1 : Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy. / Shukla, Anju; Narayanan, Dhanya L.; Asher, Urja; Girisha, Katta M.

In: Clinical Genetics, Vol. 96, No. 3, 01.01.2019, p. 276-277.

Research output: Contribution to journalLetter

TY - JOUR

T1 - A novel bi-allelic loss-of-function variant in MYOD1

T2 - Further evidence for gene-disease association and phenotypic variability in MYOD1-related myopathy

AU - Shukla, Anju

AU - Narayanan, Dhanya L.

AU - Asher, Urja

AU - Girisha, Katta M.

PY - 2019/1/1

Y1 - 2019/1/1

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U2 - 10.1111/cge.13596

DO - 10.1111/cge.13596

M3 - Letter

C2 - 31260566

AN - SCOPUS:85068762620

VL - 96

SP - 276

EP - 277

JO - Clinical Genetics

JF - Clinical Genetics

SN - 0009-9163

IS - 3

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