3 results for author:"Prat L." in Literature citations
› Repeat search in UniProtKB (1)
|Twenty-four novel mutations in Wilson disease patients of predominantly European ancestry.|
Cox D.W., Prat L., Walshe J.M., Heathcote J., Gaffney D.
|Genetic variation in the promoter and 5' UTR of the copper transporter, ATP7B, in patients with Wilson disease.|
Cullen L.M., Prat L., Cox D.W.
Clin. Genet. 64:429-432(2003) · Mapped (9)
|Tissue localization of the copper chaperone ATOX1 and its potential role in disease.|
Moore S.D., Helmle K.E., Prat L.M., Cox D.W.
Mamm. Genome 13:563-568(2002) · Mapped (1)