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p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator‐related disorders (congenital bilateral absence of vas deferens)
Authors:Donatello Salvatore M.D.  Domenico Dell'Edera B.Sc.  Carmela Colangelo M.D.  Giuseppina Smaldore B.Sc.
Affiliation:1. Cystic Fibrosis Center, Pediatric Center Bambino Gesù Basilicata, AOR Hospital San Carlo, Potenza, Italy;2. Unit of Cytogenetics and Molecular Genetics, Madonna delle Grazie Hospital, Matera, Italy;3. Laboratory of Biochemistry, AOR Hospital San Carlo, Potenza, Italy
Abstract:
Keywords:
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