Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens

OBJECTIVE: To investigate whether genetic modifiers of CF lung disease also predispose to CBAVD in association with CFTR mutations. We tested the hypothesis that polymorphisms of TGFB1 (transforming growth factor) (rs 1982073, rs 1800471) and EDNRA (endothelin receptor type A) (rs 5335, rs 1801708)...

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Bibliografiset tiedot
Päätekijät: Havasi, Viktoria, Rowe, Steven M., Kolettis, Peter N., Dayangac, Didem, Şahin, Ahmet, Grangeia, Ana, Carvalho, Filipa, Barros, Alberto, Sousa, Mario, Bassas, Lluis, Casals, Teresa, Sorscher, Eric J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2010
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3767313/
https://ncbi.nlm.nih.gov/pubmed/20100616
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.fertnstert.2009.11.044
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