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Pathol Biol (Paris). 2009 May;57(3):272-9. doi: 10.1016/j.patbio.2008.09.004. Epub 2008 Nov 28.

[From gene to disease: copper-transporting P ATPases alteration].

[Article in French]

Author information

1
Ecole du Val-de-GrĂ¢ce, 1 Place Alphonse-Laveran, 75005 Paris, France. carinegarcia92@wanadoo.fr

Abstract

Copper is a trace metal, essential for many biological processes. Copper is also toxic if in excessive amounts; its homeostatic balance requires a delicate regulation. Several severe hereditary human disorders of copper regulatory mechanisms have been identified; they are related to mutations in gene ATP7A and ATP7B coding for copper-transporting proteins. Those mutations result in copper deficiency for ATP7A (Menkes disease) and copper overload for ATP7B (Wilson disease). Usually, clinical and biochemical phenotypes of these diseases are disparate. This article focuses on the molecular pathogenesis of Wilson and Menkes disease, and discusses how causing mutations are correlated with molecular defects and disease phenotypes.

PMID:
19046832
DOI:
10.1016/j.patbio.2008.09.004
[Indexed for MEDLINE]

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