Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles
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DOI: 10.1111/andr.12592
Abstract: Congenital absence of vas deferens (CAVD) is a major cause of obstructive azoospermia. Mutations in CFTR and ADGRG2 are responsible for this disease. However, until now the genetic spectrum of the CFTR and ADGRG2 genes… read more here.
Keywords: congenital absence; vas deferens; genetic spectrum; absence vas ... See more keywords