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

• Κύριοι συγγραφείς: Rosaria Nardello (Συγγραφέας), Vincenzo Antona (Συγγραφέας), Giuseppe Donato Mangano (Συγγραφέας), Vincenzo Salpietro (Συγγραφέας), Salvatore Mangano (Συγγραφέας), Antonina Fontana (Συγγραφέας)
• Μορφή: Βιβλίο
• Έκδοση: BMC, 2021-04-01T00:00:00Z.
• Θέματα: article
• Διαθέσιμο Online: 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...