Advance in genetic research on multiple system atrophy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
;
(6): 418-421, 2015.
Artigo
em Chinês
| WPRIM
| ID: wpr-239455
ABSTRACT
Multiple system atrophy (MSA) is a progressive neurodegenerative disorder. Widespread presence of glial cytoplasmic inclusions is the neuropathologic hallmark of MSA. The disease has long been considered as a sporadic disorder. However, in recent years, a few familial cases of MSA have been reported, and researches have verified certain genetic variants could increase the risk of MSA. These indicated genetic factors may play an imported role in the pathogenesis of MSA. In this review, the emerging evidence in favor of genetic players in MSA is discussed.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Dosagem de Genes
/
Atrofia de Múltiplos Sistemas
/
Pesquisa em Genética
/
Genética
Limite:
Animais
/
Humanos
Idioma:
Chinês
Revista:
Chinese Journal of Medical Genetics
Ano de publicação:
2015
Tipo de documento:
Artigo
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