Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescence.
about
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationshipLong-chain L-3-hydroxyacyl-coenzyme a dehydrogenase deficiency: a molecular and biochemical reviewInborn errors of mitochondrial fatty acid oxidation.Performance of serum and dried blood spot acylcarnitine profiles for detection of fatty acid β-oxidation disorders in adult patients with rhabdomyolysis
P2860
Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescence.
description
1997 nî lūn-bûn
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1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
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1997年学术文章
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1997年学术文章
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1997年学术文章
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1997年学术文章
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1997年學術文章
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1997年學術文章
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name
Mitochondrial trifunctional pr ...... myoglobinuria in adolescence.
@en
Mitochondrial trifunctional pr ...... myoglobinuria in adolescence.
@nl
type
label
Mitochondrial trifunctional pr ...... myoglobinuria in adolescence.
@en
Mitochondrial trifunctional pr ...... myoglobinuria in adolescence.
@nl
prefLabel
Mitochondrial trifunctional pr ...... myoglobinuria in adolescence.
@en
Mitochondrial trifunctional pr ...... myoglobinuria in adolescence.
@nl
P2093
P356
P1433
P1476
Mitochondrial trifunctional pr ...... myoglobinuria in adolescence.
@en
P2093
Hashimoto T
Matsumoto I
Miyajima H
P304
P356
10.1212/WNL.49.3.833
P407
P577
1997-09-01T00:00:00Z