3 results for author:"Prat L." in Literature citations
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| 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) |