Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28.
about
Mitochondrial disease in adults: what's old and what's new?A neurodegenerative perspective on mitochondrial optic neuropathiesMitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease.Spectrum of combined respiratory chain defects.Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.Mutations causing mitochondrial disease: What is new and what challenges remain?MtDNA-maintenance defects: syndromes and genes.Eyelid Dysfunction in Neurodegenerative, Neurogenetic, and Neurometabolic Disease.Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation.
P2860
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P2860
Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh-hant
name
Clonal expansion of secondary ...... pinocerebellar ataxia type 28.
@en
Clonal expansion of secondary ...... pinocerebellar ataxia type 28.
@nl
type
label
Clonal expansion of secondary ...... pinocerebellar ataxia type 28.
@en
Clonal expansion of secondary ...... pinocerebellar ataxia type 28.
@nl
prefLabel
Clonal expansion of secondary ...... pinocerebellar ataxia type 28.
@en
Clonal expansion of secondary ...... pinocerebellar ataxia type 28.
@nl
P2093
P50
P1433
P1476
Clonal expansion of secondary ...... pinocerebellar ataxia type 28.
@en
P2093
Andrew M Schaefer
Douglass M Turnbull
Jessica Gabriel
Kamil Sitarz
Mark Roberts
Robert McFarland
Robert W Taylor
P304
P356
10.1001/JAMANEUROL.2014.1753
P407
P50
P577
2015-01-01T00:00:00Z