- Title
- A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
- Creators - without role
- Mutaz Amin - Al-Neelain UniversityCedric Vignal - Hôpital Robert-DebréEsraa Eltaraifee - University of KhartoumInaam N. Mohammed - University of KhartoumAhlam A. A. Hamed - University of KhartoumMaha A. Elseed - University of KhartoumArwa Babai - University of KhartoumIman Elbadi - University of KhartoumDoua Mustafa - University of KhartoumRayan Abubaker - University of KhartoumMohamed Mustafa - University of KhartoumSeverine Drunat - Hôpital Robert-DebréLiena E. O. Elsayed - Princess Nourah bint Abdulrahman UniversityAmmar E. Ahmed - University of KhartoumOdile Boespflug-Tanguy - Hôpital Robert-DebréImen Dorboz - Délégation Paris 7
- Publication Details
- BMC medical genomics, Vol.15(1), pp.1-236
- Publisher
- BioMed Central
- Identifiers
- 9927922308331
- Academic Unit
- Princess Nourah bint Abdulrahman University
- Language
- English
- Resource Type
- Journal article
Journal article
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
BMC medical genomics, Vol.15(1), pp.1-236
08/11/2022
PMID: 36348459
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