Screening for mutations in the C-terminal region of RYR1 gene identify high frequency of autosomal recessive form of central core disease (CCD) in Brazil
| Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
|---|---|
| Data(s) |
20/05/2014
20/05/2014
01/10/2005
|
| Formato |
680-680 |
| Identificador |
http://www.sciencedirect.com/science/article/pii/S0960896605001884 Neuromuscular Disorders. Oxford: Pergamon-Elsevier B.V., v. 15, n. 9-10, p. 680-680, 2005. 0960-8966 http://hdl.handle.net/11449/38788 WOS:000232221900028 |
| Idioma(s) |
eng |
| Publicador |
Elsevier B.V. |
| Relação |
Neuromuscular Disorders |
| Direitos |
closedAccess |
| Tipo |
info:eu-repo/semantics/conferenceObject |
