CFTR Mutation Analysis of a Caucasian Father with Congenital Bilateral Absence of Vas Deferens, a Taiwanese Mother, and Twins Resulting from ICSI Procedure

Cystic fibrosis (CF), caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, is one of the most common autosomal recessive diseases in Caucasians. We screened for the CFTR gene mutation in a Caucasian father with congenital bilateral absence of the vas deferens (...

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Detalhes bibliográficos

Principais autores:	Han-Sun Chiang, Chien-Chih Wu, Yi-No Wu, Jyh-Feng Lu, Gin-Hong Lin, Jiann-Loung Hwang
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Elsevier 2008-09-01
coleção:	Journal of the Formosan Medical Association
Assuntos:	CFTR mutation congenital bilateral absence of the vas deferens cystic fibrosis intracytoplasmic single sperm injection vas deferens
Acesso em linha:	http://www.sciencedirect.com/science/article/pii/S0929664608601199
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