Polymorphisms of metal transporter genes DMT1 and ATP7A in Wilson's disease.

doi:10.1016/j.jtemb.2013.08.002

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Article

Polymorphisms of metal transporter genes DMT1 and ATP7A in Wilson's disease.

Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) - 1 Jan 2014

Przybyłkowski Adam, Gromadzka Grażyna, Członkowska Anna

Abstract excerpt

Wilson's disease (WND) is an inherited disorder of copper metabolism. Divalent metal transporter1 (DMT1) and ATP7A play important roles in metal transport in humans. The frequency of two single nucleotide polymorphisms of the DMT1 gene: DMT1 IVS4 C>A, DMT1 11245 T>C and two of the ATP7A gene: rs1062472 T>C, ATP7A rs 2227291 G>C have been evaluated in a population of 108 Wilson's disease patients and 108 sex- and...

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PMID: 24120082
DOI: 10.1016/j.jtemb.2013.08.002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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