Analysis of mutations in the cystic fibrosis transmembrane regulator (CFTR) gene in patients with obstructive azoospermia
Author:
Affiliation:
1. Universidade de São Paulo, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v26n1/a01v26n1.pdf
Reference18 articles.
1. Congenital Bilateral Absence of the Vas Deferens: a primarily genital form of cystic fibrosis;Anguiano A;JAMA,1992
2. The Metabolic Basis of Inherited Disease;Beaudet A,1989
3. Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations;Bernardino ALF;Genetic testing,2000
4. The Metabolic Basis of Inherited Disease;Boat TF,1989
5. Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected;Casals T;Hum Genet,1995
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4. Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD;Andrologia;2011-07-18
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