Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles

ConclusionThis study illustrates the significance of all exon sequencing inCFTR andADGRG2. A picture of the genetic spectrum of Chinese CAVD patients and the most common mutations can be described, which are different from Caucasian cohorts and Chinese CF patients.
Source: Andrology - Category: Urology & Nephrology Authors: Tags: Original Article Source Type: research