Mutations of ATP7B gene in Wilson disease in Japan: identification of nine mutations and lack of clear founder effect in a Japanese population.

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Citation

Yamaguchi A, Matsuura A, Arashima S, Kikuchi Y, Kikuchi K

Mutations of ATP7B gene in Wilson disease in Japan: identification of nine mutations and lack of clear founder effect in a Japanese population.

Hum Mutat. 1998;Suppl 1:S320-2.

PubMed ID
9452121 [ View in PubMed
]
Abstract

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DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Copper-transporting ATPase 2P35670Details