POLG mutations in Australian patients with mitochondrial disease.
about
Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review.Hypothesis driven single nucleotide polymorphism search (HyDn-SNP-S).Co-occurrence of four nucleotide changes associated with an adult mitochondrial ataxia phenotype.Identification of a Mitochondrial DNA Polymerase Affecting Cardiotoxicity of Sunitinib Using a Genome-Wide Screening on S. pombe Deletion Library.Gastrointestinal manifestations of mitochondrial disorders: a systematic review.Novel POLG mutations and variable clinical phenotypes in 13 Italian patients.
P2860
POLG mutations in Australian patients with mitochondrial disease.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年學術文章
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name
POLG mutations in Australian patients with mitochondrial disease.
@en
POLG mutations in Australian patients with mitochondrial disease.
@nl
type
label
POLG mutations in Australian patients with mitochondrial disease.
@en
POLG mutations in Australian patients with mitochondrial disease.
@nl
prefLabel
POLG mutations in Australian patients with mitochondrial disease.
@en
POLG mutations in Australian patients with mitochondrial disease.
@nl
P2093
P2860
P1476
POLG mutations in Australian patients with mitochondrial disease.
@en
P2093
P2860
P304
P356
10.1111/J.1445-5994.2012.02847.X
P50
P577
2013-02-01T00:00:00Z