SHC2 gene copy number in multiple system atrophy (MSA)

PURPOSE: Multiple system atrophy (MSA) is a sporadic, late onset, rapidly-progressing neurodegenerative disorder, which is characterized by autonomic failure, together with parkinsonian, cerebellar, and pyramidal motor symptoms. The pathologic hallmark is the glial cytoplasmic inclusion with alpha-s...

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Detalhes bibliográficos
Main Authors: Ferguson, Marcus C., Garland, Emily M., Hedges, Lora, Womack-Nunley, Bethany, Hamid, Rizwan, Phillips, John A., Shibao, Cyndya A., Raj, Satish R., Biaggioni, Italo, Robertson, David
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3946192/
https://ncbi.nlm.nih.gov/pubmed/24170347
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10286-013-0216-8
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