Novel ADGRG2 truncating variants in patients with X ‐linked Congenital Absence of Vas Deferens
ConclusionOur results confirm the interest ofADGRG2 sequencing in patients with CAVD not formerly related to CFTR dysfunction, especially in absence of associated unilateral renal agenesis.
Source: Andrology - Category: Urology & Nephrology Authors: Adrien Pagin,
Anne Bergougnoux,
Emmanuelle Girodon,
Marie ‐Pierre Reboul,
Christelle Willoquaux,
Maryse Kesteloot,
Caroline Raynal,
Thierry Bienvenu,
Mathilde Humbert,
Guy Lalau,
Eric Bieth Tags: ORIGINAL ARTICLE Source Type: research
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