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

• Autors principals: Rosaria Nardello (Autor), Vincenzo Antona (Autor), Giuseppe Donato Mangano (Autor), Vincenzo Salpietro (Autor), Salvatore Mangano (Autor), Antonina Fontana (Autor)
• Format: Llibre
• Publicat: BMC, 2021-04-01T00:00:00Z.
• Matèries: article
• Accés en línia: 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...