Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion
Nigel F. Clarke; Leigh B. Waddell; Sandra T. Cooper; Margaret Perry; Robert L.L. Smith; Andrew J. Kornberg; Francesco Muntoni; Suzanne Lillis; Volker Straub; Kate Bushby; Michela Guglieri; Mary D. King; Michael A. Farrell; Isabelle Marty; Joel Lunardi; Nicole Monnier; Kathryn N. North
- 作者Nigel F. Clarke; Leigh B. Waddell; Sandra T. Cooper; Margaret Perry; Robert L.L. Smith; Andrew J. Kornberg; Francesco Muntoni; Suzanne Lillis; Volker Straub; Kate Bushby; Michela Guglieri; Mary D. King; Michael A. Farrell; Isabelle Marty; Joel Lunardi; Nicole Monnier; Kathryn N. North
- 卷第31卷
- 期第7期
- 印刷ISSN1059-7794
- 电子ISSN1098-1004
- 文件大小531.33KB
- 发表时间2010
- DOI10.1002/humu.21278