Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Natalie D Shaw,Harrison Brand,Zachary A Kupchinsky,Hemant Bengani,Lacey Plummer,Takako I Jones,Serkan Erdin,Kathleen A Williamson,Joe Rainger,Alexei Stortchevoi,Kaitlin Samocha,Benjamin B Currall,Donncha S Dunican,Ryan L Collins,Jason R Willer,Angela Lek,Monkol Lek,Malik Nassan,Shahrin Pereira,Tammy Kammin,Diane Lucente,Alexandra Silva,Catarina M Seabra,Colby Chiang,Yu An,Morad Ansari,Jacqueline K Rainger,Shelagh Joss,Jill Clayton Smith,Margaret F Lippincott, Sylvia S Singh,Nirav Patel, Jenny W Jing,Jennifer R Law, Nalton Ferraro,Alain Verloes,Anita Rauch,Katharina Steindl,Markus Zweier,Ianina Scheer,Daisuke Sato,Nobuhiko Okamoto,Christina Jacobsen,Jeanie Tryggestad,Steven Chernausek,Lisa A Schimmenti,Benjamin Brasseur,Claudia Cesaretti,Jose E García-Ortiz, Tatiana Pineda Buitrago,Orlando Perez Silva,Jodi D Hoffman, Wolfgang Mühlbauer,Klaus W Ruprecht,Bart L Loeys,Masato Shino,Angela M Kaindl,Chie-Hee Cho,Cynthia C Morton,Richard R Meehan,Veronica van Heyningen,Eric C Liao,Ravikumar Balasubramanian,Janet E Hall,Stephanie B Seminara,Daniel Macarthur,Steven A Moore,Koh-ichiro Yoshiura,James F Gusella,Joseph A Marsh,John M Graham Jr,Angela E Lin,Nicholas Katsanis,Peter L Jones,William F Crowley Jr,Erica E Davis,David R FitzPatrick,Michael E Talkowski

Nature Genetics（2017）

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摘要

Nat. Genet. 49, 238–248 (2017); published online 9 January 2017; corrected after print 20 March 2017 In the version of this article initially published, the legend to Figure 4c stated that only one proband without SMCHD1 mutation was tested for D4Z4 methylation pattern. However, three probands and one affected family member without SMCHD1 mutation were tested, as shown in the figure.

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Biomedicine,general,Human Genetics,Cancer Research,Agriculture,Gene Function,Animal Genetics and Genomics

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