MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.
about
Myopathology of Adult and Paediatric Mitochondrial Diseases.Novel recessive mutations in MSTO1 cause cerebellar atrophy with pigmentary retinopathy.Regulation of Mitochondrial Dynamics by Proteolytic Processing and Protein Turnover.Mitochondrial fusion and Bid-mediated mitochondrial apoptosis are perturbed by alcohol with distinct dependence on its metabolism
P2860
MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.
description
2017 nî lūn-bûn
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2017 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2017 թվականի մայիսին հրատարակված գիտական հոդված
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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name
MSTO1 is a cytoplasmic pro-mit ...... myopathy and ataxia in humans.
@ast
MSTO1 is a cytoplasmic pro-mit ...... myopathy and ataxia in humans.
@en
type
label
MSTO1 is a cytoplasmic pro-mit ...... myopathy and ataxia in humans.
@ast
MSTO1 is a cytoplasmic pro-mit ...... myopathy and ataxia in humans.
@en
prefLabel
MSTO1 is a cytoplasmic pro-mit ...... myopathy and ataxia in humans.
@ast
MSTO1 is a cytoplasmic pro-mit ...... myopathy and ataxia in humans.
@en
P2093
P2860
P50
P356
P1476
MSTO1 is a cytoplasmic pro-mit ...... myopathy and ataxia in humans
@en
P2093
David Weaver
Erin L Seifert
Maria Judit Molnar
Peter Balicza
Péter Várnai
Shamim Naghdi
Suresh K Joseph
Tibor Gyuris
P2860
P304
P356
10.15252/EMMM.201607058
P577
2017-07-01T00:00:00Z