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

• Main Authors: Rosaria Nardello (Author), Vincenzo Antona (Author), Giuseppe Donato Mangano (Author), Vincenzo Salpietro (Author), Salvatore Mangano (Author), Antonina Fontana (Author)
• 格式: 圖書
• 出版: BMC, 2021-04-01T00:00:00Z.
• 主題: article
• 在線閱讀: 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...