Worldwide Genetic Analysis of the CFTR Region

Mutations at the cystic fibrosis transmembrane conductance regulator gene (CFTR) cause cystic fibrosis, the most prevalent severe genetic disorder in individuals of European descent. We have analyzed normal allele and haplotype variation at four short tandem repeat polymorphisms (STRPs) and two sing...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Mateu, Eva, Calafell, Francesc, Lao, Oscar, Bonné-Tamir, Batsheva, Kidd, Judith R., Pakstis, Andrew, Kidd, Kenneth K., Bertranpetit, Jaume
Format: Artigo
Langue:Inglês
Publié: The American Society of Human Genetics 2001
Sujets:
Articles
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1234903/
https://ncbi.nlm.nih.gov/pubmed/11104661
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires