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.
Artículo
en Chino
| 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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Tipo de estudio:
Estudio observacional
/
Estudio pronóstico
Idioma:
Chino
Revista:
Chinese Journal of Practical Internal Medicine
Año:
2003
Tipo del documento:
Artículo
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