A rare homozygous missense mutation in ATP7B exon 19 in a case of Wilson disease.

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Majumdar R, Al-Jumah M, Zaidan R

A rare homozygous missense mutation in ATP7B exon 19 in a case of Wilson disease.

Eur Neurol. 2004;51(1):52-4. Epub 2003 Nov 21.

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14639035 [ View in PubMed
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Polypeptides
NameUniProt ID
Copper-transporting ATPase 2P35670Details