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

• 主要な著者: Rosaria Nardello (著者), Vincenzo Antona (著者), Giuseppe Donato Mangano (著者), Vincenzo Salpietro (著者), Salvatore Mangano (著者), Antonina Fontana (著者)
• フォーマット: 図書
• 出版事項: BMC, 2021-04-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: 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...