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Molecular mechanisms of statin intoleranceBiochemical Assessment of Coenzyme Q10 Deficiency.BACE-1, PS-1 and sAPPβ levels are increased in plasma from sporadic inclusion body myositis patients: surrogate biomarkers among inflammatory myopathies.A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency.Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q10 Deficiency in a Female Sib-Pair.
P2860
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2014年の論文
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2014年学术文章
@wuu
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
name
Biochemical diagnosis of coenzyme q10 deficiency.
@ast
Biochemical diagnosis of coenzyme q10 deficiency.
@en
type
label
Biochemical diagnosis of coenzyme q10 deficiency.
@ast
Biochemical diagnosis of coenzyme q10 deficiency.
@en
prefLabel
Biochemical diagnosis of coenzyme q10 deficiency.
@ast
Biochemical diagnosis of coenzyme q10 deficiency.
@en
P2093
P2860
P356
P1476
Biochemical diagnosis of coenzyme q10 deficiency.
@en
P2093
Iain P Hargreaves
John M Land
Rafael Artuch
Raquel Montero
Simon J R Heales
P2860
P304
P356
10.1159/000362390
P50
P577
2014-07-01T00:00:00Z