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

• Egile Nagusiak: Rosaria Nardello (Egilea), Vincenzo Antona (Egilea), Giuseppe Donato Mangano (Egilea), Vincenzo Salpietro (Egilea), Salvatore Mangano (Egilea), Antonina Fontana (Egilea)
• Formatua: Liburua
• Argitaratua: BMC, 2021-04-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: 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...