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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Detaylı Bibliyografya
Asıl Yazarlar: Mateu, Eva, Calafell, Francesc, Lao, Oscar, Bonné-Tamir, Batsheva, Kidd, Judith R., Pakstis, Andrew, Kidd, Kenneth K., Bertranpetit, Jaume
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The American Society of Human Genetics 2001
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Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1234903/
https://ncbi.nlm.nih.gov/pubmed/11104661
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