Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency.
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Mitochondrial cardioencephalopathy due to a COQ4 mutation.Estimating the occurrence of primary ubiquinone deficiency by analysis of large-scale sequencing data.Coenzyme Q10 Supplementation in Aging and Disease.Coenzyme Q10 deficiency due to a COQ4 gene defect causes childhood-onset spinocerebellar ataxia and stroke-like episodes
P2860
Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency.
description
2017 nî lūn-bûn
@nan
2017 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2017年の論文
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2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
Novel recessive mutations in C ...... ociated with CoQ10 deficiency.
@ast
Novel recessive mutations in C ...... ociated with CoQ10 deficiency.
@en
type
label
Novel recessive mutations in C ...... ociated with CoQ10 deficiency.
@ast
Novel recessive mutations in C ...... ociated with CoQ10 deficiency.
@en
prefLabel
Novel recessive mutations in C ...... ociated with CoQ10 deficiency.
@ast
Novel recessive mutations in C ...... ociated with CoQ10 deficiency.
@en
P2093
P2860
P1476
Novel recessive mutations in C ...... ociated with CoQ10 deficiency.
@en
P2093
Ali B Naini
Catarina Maria Quinzii
Gino R Somers
Jane Dunning Broadbent
Jessie M Cameron
Marcello Ziosi
Neal Sondheimer
Stacy Hewson
P2860
P356
10.1016/J.YMGMR.2017.05.001
P577
2017-05-11T00:00:00Z