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Article

A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene.

CNS neuroscience & therapeutics - 1 Nov 2012

Zhao Zhang-Ning, Bao Meng-Xin, Ma Gao-Ting, Liu Xiao-Min, Xu Wen-Juan, Sun Zhong-Wen, Chen Huan, Zhu Mei-Jia

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Share to Electron-Transferring Flavoproteins
Share to Iron-Sulfur Proteins
Share to Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Oxidoreductases Acting on CH-NH Group Donors

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Identifiers

PMID: 23106979
DOI: 10.1111/cns.12007
PMCID: PMC6493656

Genes

ETFDH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

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A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene.PMID 23106979Read ↗

Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiencySemantic proximity Read ↗

A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency (MADD) with a novel mutation in ETFDH gene.Semantic proximity Read ↗

Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patients.Semantic proximity Read ↗

Clinical characteristics and gene mutation analysis of an adult patient with ETFDH‑related multiple acyl‑CoA dehydrogenase deficiency.Semantic proximity Read ↗

ETF dehydrogenase advances in molecular genetics and impact on treatment.Semantic proximity Read ↗

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.Semantic proximity Read ↗

Multiple acyl-coenzyme A dehydrogenation disorders (MAD) responsive to riboflavin: biochemical studies in fibroblasts.Semantic proximity Read ↗

[Multiple acyl-coA dehydrogenase deficiency caused by new variant of ETFDH gene in 2 children].Semantic proximity Read ↗

Flavin adenine dinucleotide synthase deficiency due to FLAD1 mutation presenting as multiple acyl-CoA dehydrogenation deficiency-like disease: A case reportSemantic proximity Read ↗

Amelioration of acylcarnitine profile using bezafibrate and riboflavin in a case of adult-onset glutaric acidemia type 2 with novel mutations of the electron transfer flavoprotein dehydrogenase (ETFDH) gene.Semantic proximity Read ↗

Update on clinical aspects and treatment of selected vitamin-responsive disorders II (riboflavin and CoQ 10).Semantic proximity Read ↗

Hyperhomocysteinemia in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

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