Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency.
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SPG20 mutation in three siblings with familial hereditary spastic paraplegia.The Relationship between Mitochondrial Respiratory Chain Activities in Muscle and Metabolites in Plasma and Urine: A Retrospective Study.Mitochondrial energy metabolism is required for lifespan extension by the spastic paraplegia-associated protein spartin.Novel SPG20 mutation in an extended family with Troyer syndrome.The role of TGF-β superfamily signaling in neurological disorders.
P2860
Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency.
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2016 nî lūn-bûn
@nan
2016 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Novel Homozygous Missense Muta ...... tochrome c Oxidase Deficiency.
@ast
Novel Homozygous Missense Muta ...... tochrome c Oxidase Deficiency.
@en
type
label
Novel Homozygous Missense Muta ...... tochrome c Oxidase Deficiency.
@ast
Novel Homozygous Missense Muta ...... tochrome c Oxidase Deficiency.
@en
prefLabel
Novel Homozygous Missense Muta ...... tochrome c Oxidase Deficiency.
@ast
Novel Homozygous Missense Muta ...... tochrome c Oxidase Deficiency.
@en
P2093
P2860
P356
P1476
Novel Homozygous Missense Muta ...... tochrome c Oxidase Deficiency.
@en
P2093
Avraham Shaag
Devorah Soiferman
Orly Elpeleg
Stavit Shalev
P2860
P356
10.1007/8904_2016_580
P577
2016-08-19T00:00:00Z