Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation.

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Pendlebury ST, Rothwell PM, Dalton A, Burton EA

Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation.

Neurology. 2004 Nov 23;63(10):1982-3.

PubMed ID
15557537 [ View in PubMed
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Polypeptides
NameUniProt ID
Copper-transporting ATPase 2P35670Details