Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens | Zendy

Ana Grangeia | Zendy; Florence Niel | Zendy; Filipa Carvalho | Zendy; Susana Fernandes | Zendy; Azarnouche Ardalan | Zendy; Emmanuelle Girodon | Zendy; Joaquina Silva | Zendy; L. L. Ferrás | Zendy; Mário Sousa | Zendy; Alberto Barros | Zendy

Open Access

Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens

Author(s) -

Ana Grangeia,

Florence Niel,

Filipa Carvalho,

Susana Fernandes,

Azarnouche Ardalan,

Emmanuelle Girodon,

Joaquina Silva,

L. L. Ferrás,

Mário Sousa,

Alberto Barros

Publication year - 2004

Publication title -

human reproduction

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.446

H-Index - 226

eISSN - 1460-2350

pISSN - 0268-1161

DOI - 10.1093/humrep/deh462

Subject(s) - cystic fibrosis transmembrane conductance regulator , azoospermia , vas deferens , obstructive azoospermia , biology , cystic fibrosis , population , allele , genetics , allele frequency , male infertility , medicine , microbiology and biotechnology , endocrinology , infertility , gene , pregnancy , environmental health

Cystic fibrosis conductance transmembrane regulator (CFTR) gene mutations and IVS8 poly(T) variants in Portuguese patients with bilateral (CBAVD) and unilateral (CUAVD) congenital absence of the vas deferens remain to be evaluated.

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