Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations.

Because defects in the phenylalanine hydroxylase gene (PAH) cause phenylketonuria (PKU), PAH was studied for normal polymorphisms and linkage disequilibrium soon after the gene was cloned. Studies in the 1980s concentrated on European populations in which PKU was common and showed that haplotype-fre...

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Autors principals: Kidd, J R, Pakstis, A J, Zhao, H, Lu, R B, Okonofua, F E, Odunsi, A, Grigorenko, E, Tamir, B B, Friedlaender, J, Schulz, L O, Parnas, J, Kidd, K K
Format: Artigo
Idioma:Inglês
Publicat: 2000
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378054/
https://ncbi.nlm.nih.gov/pubmed/10788337
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