• PMID: 10878476
• Gene Name: CFTR
• Condition: Congenital bilateral absence of the vas deferens (CBAVD)
• Association: Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR gene in a patient with congenitalbilateral absence of the vas deferens.
• Mutation: R766M, R792G
• Sex: Male
• Infertility type: Male infertility
• Other associated phenotypes: Congenital bilateral absence of the vas deferens (CBAVD)

Two novel missense mutations (R766M and R792G) in exon 13 of the CFTR gene in a patient with congenital bilateral absence of the vas deferens

Ravnik-Glavac M, Dean M, Glavac D.

No abstract available