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...

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Xehetasun bibliografikoak
Egile Nagusiak: Mateu, Eva, Calafell, Francesc, Lao, Oscar, Bonné-Tamir, Batsheva, Kidd, Judith R., Pakstis, Andrew, Kidd, Kenneth K., Bertranpetit, Jaume
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: The American Society of Human Genetics 2001
Gaiak:
Articles
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1234903/
https://ncbi.nlm.nih.gov/pubmed/11104661
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