Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause i...
Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome
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Shaw, Natalie D , Brand, Harrison , Kupchinsky, Zachary A , Bengani, Hemant , Plummer, Lacey , Jones, Takako I , Erdin, Serkan , Williamson, Kathleen A , Rainger, Joe , Stortchevoi, Alexei , Samocha, Kaitlin , Currall, Benjamin B , Dunican, Donncha S , Collins, Ryan L , Willer, Jason R , Lek, Angela , Lek, Monkol , Nassan, Malik , Pereira, Shahrin , Kammin, Tammy , Lucente, Diane , Silva, Alexandra , Seabra, Catarina M , Chiang, Colby , An, Yu , Ansari, Morad , Rainger, Jacqueline K , Joss, Shelagh , Smith, Jill Clayton , Lippincott, Margaret F , Singh, Sylvia S , Patel, Nirav , Jing, Jenny W , Law, Jennifer R , Ferraro, Nalton , Verloes, Alain , Rauch, Anita , Steindl, Katharina , Zweier, Markus , Scheer, Ianina , Sato, Daisuke , Okamoto, Nobuhiko , Jacobsen, Christina , Tryggestad, Jeanie , Chernausek, Steven , Schimmenti, Lisa A , Brasseur, Benjamin , Cesaretti, Claudia , García-Ortiz, Jose E , Buitrago, Tatiana Pineda , Silva, Orlando Perez , Hoffman, Jodi D , Mühlbauer, Wolfgang , Ruprecht, Klaus W , Loeys, Bart L , Shino, Masato , Kaindl, Angela M , Cho, Chie-Hee , Morton, Cynthia C , Meehan, Richard R , van Heyningen, Veronica , Liao, Eric C , Balasubramanian, Ravikumar , Hall, Janet E , Seminara, Stephanie B , Macarthur, Daniel , Moore, Steven A , Yoshiura, Koh-ichiro , Gusella, James F , Marsh, Joseph A , Graham, John M , Lin, Angela E , Katsanis, Nicholas , Jones, Peter L , Crowley, William F , Davis, Erica E , FitzPatrick, David R and Talkowski, Michael E
Publisher
New York: Nature Publishing Group US
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English
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Publisher
New York: Nature Publishing Group US
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Contents
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...
Alternative Titles
Full title
Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome
Authors, Artists and Contributors
Author / Creator
Brand, Harrison
Kupchinsky, Zachary A
Bengani, Hemant
Plummer, Lacey
Jones, Takako I
Erdin, Serkan
Williamson, Kathleen A
Rainger, Joe
Stortchevoi, Alexei
Samocha, Kaitlin
Currall, Benjamin B
Dunican, Donncha S
Collins, Ryan L
Willer, Jason R
Lek, Angela
Lek, Monkol
Nassan, Malik
Pereira, Shahrin
Kammin, Tammy
Lucente, Diane
Silva, Alexandra
Seabra, Catarina M
Chiang, Colby
An, Yu
Ansari, Morad
Rainger, Jacqueline K
Joss, Shelagh
Smith, Jill Clayton
Lippincott, Margaret F
Singh, Sylvia S
Patel, Nirav
Jing, Jenny W
Law, Jennifer R
Ferraro, Nalton
Verloes, Alain
Rauch, Anita
Steindl, Katharina
Zweier, Markus
Scheer, Ianina
Sato, Daisuke
Okamoto, Nobuhiko
Jacobsen, Christina
Tryggestad, Jeanie
Chernausek, Steven
Schimmenti, Lisa A
Brasseur, Benjamin
Cesaretti, Claudia
García-Ortiz, Jose E
Buitrago, Tatiana Pineda
Silva, Orlando Perez
Hoffman, Jodi D
Mühlbauer, Wolfgang
Ruprecht, Klaus W
Loeys, Bart L
Shino, Masato
Kaindl, Angela M
Cho, Chie-Hee
Morton, Cynthia C
Meehan, Richard R
van Heyningen, Veronica
Liao, Eric C
Balasubramanian, Ravikumar
Hall, Janet E
Seminara, Stephanie B
Macarthur, Daniel
Moore, Steven A
Yoshiura, Koh-ichiro
Gusella, James F
Marsh, Joseph A
Graham, John M
Lin, Angela E
Katsanis, Nicholas
Jones, Peter L
Crowley, William F
Davis, Erica E
FitzPatrick, David R
Talkowski, Michael E
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Primary Identifiers
Record Identifier
TN_cdi_crossref_primary_10_1038_ng0617_969c
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1038_ng0617_969c
Other Identifiers
ISSN
1061-4036
E-ISSN
1546-1718
DOI
10.1038/ng0617-969c
