Molecular-genetic causes for the high frequency of phenylketonuria in the population from the North Caucasus

Phenylketonuria is an inherited disease caused by mutations in the phenylalanine hydroxylase gene PAH. Different PAH pathogenic variants occur in different ethnic groups with various frequencies and the incidence of the disease itself varies from country to country. In the Caucasus region of Russia,...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:PLoS One
Autori principali: Gundorova, Polina, Zinchenko, Rena A., Kuznetsova, Irina A., Bliznetz, Elena A., Stepanova, Anna A., Polyakov, Aleksander V.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2018
Soggetti:
Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6070269/
https://ncbi.nlm.nih.gov/pubmed/30067850
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0201489
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi