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

• Hauptverfasser: Rosaria Nardello (Verfasst von), Vincenzo Antona (Verfasst von), Giuseppe Donato Mangano (Verfasst von), Vincenzo Salpietro (Verfasst von), Salvatore Mangano (Verfasst von), Antonina Fontana (Verfasst von)
• Format: Buch
• Veröffentlicht: BMC, 2021-04-01T00:00:00Z.
• Schlagworte: article
• Online-Zugang: 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...