A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability

• Main Authors: Mutaz Amin (Author), Cedric Vignal (Author), Esraa Eltaraifee (Author), Inaam N. Mohammed (Author), Ahlam A. A. Hamed (Author), Maha A. Elseed (Author), Arwa Babai (Author), Iman Elbadi (Author), Doua Mustafa (Author), Rayan Abubaker (Author), Mohamed Mustafa (Author), Severine Drunat (Author), Liena E. O. Elsayed (Author), Ammar E. Ahmed (Author), Odile Boespflug-Tanguy (Author), Imen Dorboz (Author)
• Format: Book
• Published: BMC, 2022-11-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background The etiology of intellectual disabilities is diverse and includes both genetic and environmental factors. The genetic causes of intellectual disabilities range from chromosomal aberrations to single gene disorders. The TRAPPC9 gene has been reported to cause autosomal recessive f...