The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy.
about
Mosaicism of mitochondrial genetic variation in atherosclerotic lesions of the human aorta.Endocrine manifestations related to inherited metabolic diseases in adults.Mitochondrial Copy Number and D-Loop Variants in Pompe Patients.Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: an overview study.Targeting mitochondrial function to protect against vision loss.Clinical utility gene card for: Wolfram syndrome.
P2860
The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年學術文章
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2011年學術文章
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2011年學術文章
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name
The mitochondrial ND1 m.3337G> ...... m syndrome and cardiomyopathy.
@en
The mitochondrial ND1 m.3337G> ...... m syndrome and cardiomyopathy.
@nl
type
label
The mitochondrial ND1 m.3337G> ...... m syndrome and cardiomyopathy.
@en
The mitochondrial ND1 m.3337G> ...... m syndrome and cardiomyopathy.
@nl
prefLabel
The mitochondrial ND1 m.3337G> ...... m syndrome and cardiomyopathy.
@en
The mitochondrial ND1 m.3337G> ...... m syndrome and cardiomyopathy.
@nl
P2093
P1476
The mitochondrial ND1 m.3337G> ...... m syndrome and cardiomyopathy.
@en
P2093
Emna Mkaouar-Rebai
Faiza Fakhfakh
Ikhlass Haj Salem
Mohamed Abid
Mouna Mnif
Nadia Charfi
Najla Mezghani
Nozha Kallel
P304
P356
10.1016/J.BBRC.2011.06.106
P407
P577
2011-06-23T00:00:00Z