Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies

BACKGROUND & OBJECTIVES: The role of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in congenital bilateral absence of vas deferens and unilateral renal agenesis (CBAVD-URA) has been controversial. Here, we report the cases of five Indian males with CBAVD-URA. The obje...

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Vydáno v:Indian J Med Res
Hlavní autoři: Gajbhiye, Rahul, Kadam, Kaushiki, Khole, Aalok, Gaikwad, Avinash, Kadam, Seema, Shah, Rupin, Kumaraswamy, Rangaswamy, Khole, Vrinda
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2016
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4989835/
https://ncbi.nlm.nih.gov/pubmed/27488005
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-5916.187110
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