Progress of myostatin on duchenne muscular dystrophy / 国际儿科学杂志
International Journal of Pediatrics
;
(6): 356-359, 2019.
Artigo
em Chinês
| WPRIM
| ID: wpr-751468
ABSTRACT
Duchenne muscular dystrophy (DMD) is a severe muscular genetic disorder,which is caused by a mutation in the DMD gene encoding the dystrophin protein.The clinical manifestation of DMD is the progressive muscular dystrophy.Myostatin is a negative regulator of skeletal muscle growth and development.In recent years,it has received extensive attention in the treatment of muscle diseases.This review focuses on the structural and activity of myostatin,its regulation of skeletal muscle growth and noval approaches to Myostatin inhibitor in the treatment of DMD.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Idioma:
Chinês
Revista:
International Journal of Pediatrics
Ano de publicação:
2019
Tipo de documento:
Artigo
Similares
MEDLINE
...
LILACS
LIS