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Significance of CFTR gene mutations in patients with congenital aplasia of vas deferens with special regard to renal aplasia

✍ Scribed by J. U. Schwarzer; M. Schwarz


Book ID
115137739
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
57 KB
Volume
44
Category
Article
ISSN
0303-4569

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Several recent studies have demonstrated the presence of mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene in healthy males with infertility caused by congenital absence of the vas deferens (CBAVD), previously recognized as an idiopathic genetic condition distinct from