A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder.
about
De novo mtDNA point mutations are common and have a low recurrence risk.Mitochondrial ATP synthase: architecture, function and pathology.Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: an overview study.Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.Polymorphisms of mitochondrial ATPase 8/6 genes and association with milk production traits in Holstein cows.ATP Synthase Diseases of Mitochondrial Genetic Origin.
P2860
A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
A de novo mutation in the aden ...... t with mitochondrial disorder.
@en
A de novo mutation in the adenosine triphosphatase
@nl
type
label
A de novo mutation in the aden ...... t with mitochondrial disorder.
@en
A de novo mutation in the adenosine triphosphatase
@nl
prefLabel
A de novo mutation in the aden ...... t with mitochondrial disorder.
@en
A de novo mutation in the adenosine triphosphatase
@nl
P2093
P2860
P356
P1476
A de novo mutation in the aden ...... t with mitochondrial disorder.
@en
P2093
Chahnez Triki
Emna Mkaouar-Rebai
Faiza Fakhfakh
Fatma Kammoun
Imen Chamkha
Ines Hsairi
Nadège Kammoun
P2860
P304
P356
10.1177/0883073809344351
P577
2010-03-04T00:00:00Z