SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.
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Genetic and phenotypic characterization of complex hereditary spastic paraplegiaOvercoming the divide between ataxias and spastic paraplegias: Shared phenotypes, genes, and pathways.Loss of the Drosophila m-AAA mitochondrial protease paraplegin results in mitochondrial dysfunction, shortened lifespan, and neuronal and muscular degeneration.Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China.
P2860
SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.
@en
type
label
SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.
@en
altLabel
SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases
@en
prefLabel
SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.
@en
P2093
P2860
P50
P356
P1476
SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.
@en
P2093
Care4Rare Canada Consortium
Jacek Majewski
Karine Choquet
Marie-France Rioux
Marie-Josée Dicaire
Martine Tétreault
Megan R Vanstone
Roberta La Piana
Sharon Yang
P2860
P2888
P304
P356
10.1038/EJHG.2015.240
P407
P577
2015-12-02T00:00:00Z
P5875
P6179
1007113612