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Article

Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathy.

Postgraduate medical journal - 1 Jun 2006

Kumar N, Gross J B

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Share to Adenosine Triphosphatases
Share to Cation Transport Proteins
Share to Copper
Share to Copper-Transporting ATPases

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 16754714
DOI: 10.1136/pgmj.2005.043505
PMCID: PMC2563737

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathy.PMID 16754714Read ↗

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