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PMID: 16283886 Published · ppublish English Comparative Study Letter Research Support, Non-U.S. Gov't

COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology.

Clinical genetics ·Vol. 68 ·No. 6 ·2005-12-00 ·Pages 548-51

Coronado VA, Bonneville JA, Nazer H, Roberts EA, Cox DW

Abstract

暂无摘要

MeSH Terms

Adaptor Proteins, Signal Transducing Adenosine Triphosphatases/genetics Carrier Proteins Cation Transport Proteins/genetics Copper/metabolism Copper-Transporting ATPases DNA Mutational Analysis Genetic Testing/methods Haplotypes/genetics Hepatolenticular Degeneration/genetics Humans Metabolic Diseases/genetics,metabolism Pedigree Phenotype Proteins/genetics Sequence Analysis, DNA

Chemicals

Adaptor Proteins, Signal Transducing COMMD1 protein, human Carrier Proteins Cation Transport Proteins Proteins Copper Adenosine Triphosphatases Copper-Transporting ATPases

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

Coronado V A

Bonneville J A

Nazer H

Roberts E A

Cox D W

Article Info

Journal

Clinical genetics

Abbr.

Clin Genet

ISSN

0009-9163

DOI

10.1111/j.1399-0004.2005.00524.x

Published

2005-12-00

Pages

548-51

Language

English

Region

Denmark

NLM ID

0253664

Subset

External Links

PubMed source DOI: 10.1111/j.1399-0004.2005.00524.x View journal details

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COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology.

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