A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes

• Auteurs principaux: Rosaria Nardello (Auteur), Vincenzo Antona (Auteur), Giuseppe Donato Mangano (Auteur), Vincenzo Salpietro (Auteur), Salvatore Mangano (Auteur), Antonina Fontana (Auteur)
• Format: Livre
• Publié: BMC, 2021-04-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

Abstract Background Most studies relative to Y chromosome abnormalities are focused on the sexual developmental disorders. Recently, a few studies suggest that some genes located on Y chromosome may be related to different neurodevelopment disorders. Case presentation We report a child with sexual d...