Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease.

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Citation

Barada K, Nemer G, ElHajj II, Touma J, Cortas N, Boustany RM, Usta J

Early and severe liver disease associated with homozygosity for an exon 7 mutation, G691R, in Wilson's disease.

Clin Genet. 2007 Sep;72(3):264-7.

PubMed ID
17718866 [ View in PubMed
]
Abstract

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DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Copper-transporting ATPase 2P35670Details