TY  - JOUR
T1  - Missense mutations of ACTA1 cause dominant congenital myopathy with cores
A1  - Kaindl, A
LA  - English
PB  - BMJ Group
YR  - 2004
UL  - http://buscaintegrada.pucsp.br/vufind/Record/pubmed-1735626
AB  - 
KW  - Letter to JMG
ER  -