p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens)

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Published in:International journal of urology 2015-08, Vol.22 (8), p.803-804
Main Authors: Salvatore, Donatello, Dell'Edera, Domenico, Colangelo, Carmela, Smaldore, Giuseppina
Format: Article
Language:English
Subjects:
Adult
Cystic Fibrosis - genetics
Cystic Fibrosis Transmembrane Conductance Regulator - genetics
Humans
Male
Male Urogenital Diseases - complications
Mutation
Vas Deferens - abnormalities
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creator Salvatore, Donatello
Dell'Edera, Domenico
Colangelo, Carmela
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description
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source Wiley-Blackwell Read & Publish Collection
subjects Adult
Cystic Fibrosis - genetics
Cystic Fibrosis Transmembrane Conductance Regulator - genetics
Humans
Male
Male Urogenital Diseases - complications
Mutation
Vas Deferens - abnormalities
title p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens)
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