Erratum: PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families (Genet Med (2021) 23(2415-2425))(s41436021012966)(10.1038/s41436-021-01296-6))

Anne Guimier, Melanie T. Achleitner, Anne Moreau de Bellaing, Matthew Edwards, Loïc de Pontual, Kirti Mittal, Kyla E. Dunn, Megan E. Grove, Carolyn J. Tysoe, Clémantine Dimartino, Jessie Cameron, Anil Kanthi, Anju Shukla, Florence van den Broek, Diptendu Chatterjee, Charlotte L. Alston, Charlotte V. Knowles, Laura Brett, Jan A. Till, Tessa HomfrayPaul French, Georgia Spentzou, Noha A. Elserafy, Kate S. Lichkus, Bindu P. Sankaran, Hannah L. Kennedy, Peter M. George, Alexa Kidd, Saskia B. Wortmann, Dianna G. Fisk, Tamara T. Koopmann, Muhammad A. Rafiq, Jason D. Merker, Sumith Parikh, Priyanka Ahimaz, Robert G. Weintraub, Alan S. Ma, Christian Turner, Carolyn J. Ellaway, Liza K. Phillips, David R. Thorburn, Wendy K. Chung, Sajel L. Kana, Ona M. Faye-Petersen, Michelle L. Thompson, Alexandre Janin, Karen McLeod, Ruth McGowan, Robert McFarland, Katta M. Girisha, Deborah J. Morris-Rosendahl, Anna C.E. Hurst, Claire L.S. Turner, Robert M. Hamilton, Robert W. Taylor, Fanny Bajolle, Christopher T. Gordon, Jeanne Amiel, Johannes A. Mayr, Kit Doudney

Research output: Contribution to journalArticlepeer-review

Abstract

Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/s41436-021-01296-6 In the article “PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families” by Guimier A et al (Genet Med 2021;23:2415-2425), the name Sumit Parikh was spelled incorrectly.

Original languageEnglish
Pages (from-to)967
Number of pages1
JournalGenetics in medicine : official journal of the American College of Medical Genetics
Volume24
Issue number4
DOIs
Publication statusPublished - 01-04-2022

All Science Journal Classification (ASJC) codes

  • Genetics(clinical)

Fingerprint

Dive into the research topics of 'Erratum: PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families (Genet Med (2021) 23(2415-2425))(s41436021012966)(10.1038/s41436-021-01296-6))'. Together they form a unique fingerprint.

Cite this