Mutation analysis of the cystic fibrosis transmembrane conductance regulator gene in Chinese congenital absence of vas deferens patients
Author:
Funder
National Natural Science Foundation of China
Guangdong Basic and Applied Basic Research Foundation
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference31 articles.
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3. Recommendations for the classification of diseases as CFTR-related disorders;Bombieri;J. Cyst. Fibros.,2011
4. The role of SLC9A3 in Taiwanese patients with congenital bilateral absence of vas deferens (CBAVD);Chiang;J. Formos. Med. Assoc.,2019
5. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens;Chillon;N. Engl. J. Med.,1995
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