Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens - Patat, Olivier; Pagin, Adrien; Siegfried, Aurore; Mitchell, Valérie; Chassaing, Nicolas; Faguer, Stanislas; Monteil, Laetitia; Gaston, Véronique; Bujan, Louis; Courtade-Saïdi, Monique; Marcelli, François; Lalau, Guy; et al. (American journal of human genetics, 2016)
Keywords: Cell adhesion & migration; Congenital diseases; Cystic Fibrosis Transmembrane Conductance Regulator - genetics; DNA Mutational Analysis; Exome - genetics; Female; Gene Deletion; Genes, X-Linked - genetics; Genomics; Genotype & phenotype; Humans; Infertility; Life Sciences; Male; Male Urogenital Diseases - genetics; Mutation; Pedigree; Receptors, G-Protein-Coupled - genetics; Reproductive Biology; Sperm; Vas Deferens - abnormalities