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

Int J Urol. 2015 Aug;22(8):804. doi: 10.1111/iju.12823. Epub 2015 May 25.

Authors

Giuseppe Castaldo^{1

2}, Felice Amato^{3

4}

Affiliations

¹ Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy. giuseppe.castaldo@unina.it.
² CEINGE-Advanced Biotechnology Scarl, Naples, Italy. giuseppe.castaldo@unina.it.
³ Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
⁴ CEINGE-Advanced Biotechnology Scarl, Naples, Italy.

PMID: 26010140
DOI: 10.1111/iju.12823

No abstract available

Publication types

Editorial
Comment

MeSH terms

Cystic Fibrosis / genetics*
Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
Humans
Male
Male Urogenital Diseases / complications*
Vas Deferens / abnormalities*

Substances

Cystic Fibrosis Transmembrane Conductance Regulator