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Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene.

The HindIII RFLP in the human phenylalanine hydroxylase (PAH) gene is caused by the presence of an AT-rich (70%) minisatellite region. This region contains various multiple of 30-bp tandem repeats and is located 3 kb downstream of the final exon of the gene. PCR-mediated amplification of this region...

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Detalhes bibliográficos
Main Authors: Goltsov, A A, Eisensmith, R C, Konecki, D S, Lichter-Konecki, U, Woo, S L
Formato: Artigo
Idioma:Inglês
Publicado em: 1992
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682705/
https://ncbi.nlm.nih.gov/pubmed/1353941
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