Inherited progressive limb-girdle muscular dystrophy type 2A (calpainopathy): a review of literature

The Russian literature gives inadequate attention to the problem of one of the most common form of autosomal recessive progressive limb-girdle muscular dystrophies type 2A (LGMD2A) (calpainopathy). This paper highlights current views on the physiological role of calpain 3 protein, possible pathogene...

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Detalhes bibliográficos
Main Authors: D. A. Grishina, N. A. Suponeva, V. V. Shvedkov, A. V. Belopasova
Formato: Artigo
Idioma:Russo
Publicado em: ABV-press 2015-05-01
Colecção:Nervno-Myšečnye Bolezni
Assuntos:
progressive limb-girdle muscular dystrophy
calpainopathy
calpain 3
inherited myopathy
creatinine phosphokinase
electromyography
muscle magnetic resonance imaging
genetic analysis
muscle biopsy
differential diagnosis
Acesso em linha:https://nmb.abvpress.ru/jour/article/view/107
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