Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene associated myopathies
Article first published online: 13 JUL 2012
© 2012 Wiley Periodicals, Inc.
Volume 33, Issue 8, page 1310, August 2012
How to Cite
- Issue published online: 13 JUL 2012
- Article first published online: 13 JUL 2012
Vol. 33, Issue 6, 981–988, Article first published online: 4 APR 2012
The original article to which this Erratum refers was published in Human Mutation 33(6):981–988 (DOI 10.1002/humu.22056).
The authors noted some errors in the Supporting Information for this article:
In Supp. Table S1b, it is family 42 instead of 41 that has previously been published by Zhou and in family 42, the previously published mutation c.325C>T; p.Arg109Trp was found in addition to the three mutations that we have reported. These changes are in trans.
There is also a nomenclature error in (misspelling of) one mutation in patient 48: it is c.3196delT; p.Ser1066fs.
The authors regret the errors.