[Complex I deficiency due to NDUFS8 gene mutation].

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Article

[Complex I deficiency due to NDUFS8 gene mutation].

Nihon rinsho. Japanese journal of clinical medicine - 1 Apr 2002

Ito Michinori

Abstract excerpt

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Topics

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Share to Diagnosis, Differential
Share to Electron Transport Complex I
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to NAD(P)H Dehydrogenase (Quinone)

Share to NADH Dehydrogenase

Share to NADH, NADPH Oxidoreductases

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Source

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Identifiers

PMID: 12013907

Genes

NDUFS8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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[C9 deficiency].Semantic proximity Read ↗

Biallelic mutations in NDUFA8 cause complex I deficiency in two siblings with favorable clinical evolution.Semantic proximity Read ↗

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