Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD).

Subjects :: Congenital Abnormalities genetics
Cystic Fibrosis complications
Cystic Fibrosis genetics
DNA Mutational Analysis
Frameshift Mutation genetics
Humans
Male
Cystic Fibrosis Transmembrane Conductance Regulator genetics
Mutation genetics
Vas Deferens abnormalities

Language :: English
ISSN :: 1059-7794
Volume :: 9
Issue :: 2
Database :: MEDLINE
Journal :: Human mutation
Publication Type :: Academic Journal
Accession number :: 9067761
Full Text :: https://doi.org/10.1002/(SICI)1098-1004(1997)9:2<183::AID-HUMU13>3.0.CO;2-Z

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