Mutation analysis of dystrophin gene and clinical evaluation of phenotypes in X-linked dilated cardiomyopathy / 中国实用内科杂志
Chinese Journal of Practical Internal Medicine
;
(12)2003.
Artigo
em Chinês
| WPRIM
| ID: wpr-554611
ABSTRACT
T is the etiologic mutation in this family.Screening of female carrier state and follow-up study of the confirmed carriers are important for X-liked DCM family.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo observacional
/
Estudo prognóstico
Idioma:
Chinês
Revista:
Chinese Journal of Practical Internal Medicine
Ano de publicação:
2003
Tipo de documento:
Artigo
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