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Article

Oligosymptomatic adrenomyeloneuropathy due to a novel mutation in the ABCD1 start codon.

Journal of the neurological sciences - 15 Aug 2016

Dunkl Veronika, Rau Isabella, Wunderlich Gilbert, Fink Gereon R, Lehmann Helmar C

Abstract excerpt

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Topics

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Share to Adrenoleukodystrophy
Share to ATP Binding Cassette Transporter, Subfamily D, Member 1
Share to ATP-Binding Cassette Transporters

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Codon, Initiator

Share to ABCD1 gene

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Share to Paraparesis, Spastic

Source

Identifiers

PMID: 27423567
DOI: 10.1016/j.jns.2016.05.047

Genes

ABCD1

Provenance

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

Related research

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Oligosymptomatic adrenomyeloneuropathy due to a novel mutation in the ABCD1 start codon.PMID 27423567Read ↗

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Multiple endocrine disorders associated with adrenomyeloneuropathy and a novel mutation of the ABCD1 gene.Semantic proximity Read ↗

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