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Publications by Tawfiq Froukh
Mutations in MBOAT7 , Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
American Journal of Human Genetics
Genetics
Related publications
Pachygyria-Intellectual Disability-Epilepsy Syndrome
X-Linked Spasticity-Intellectual Disability-Epilepsy Syndrome
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
American Journal of Human Genetics
Genetics
Concept Formation in a Child With an Intellectual Disability and Autistic Traits
The Japanese Journal of Special Education
Genetic and Neurodevelopmental Spectrum ofSYNGAP1-associated Intellectual Disability and Epilepsy
Journal of Medical Genetics
Genetics
Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability
American Journal of Human Genetics
Genetics
Perampanel and Challenging Behaviour in Intellectual Disability and Epilepsy: A Management Dilemma
Case Reports in Psychiatry
Psychiatry
Mental Health
Severe Intellectual Disability-Epilepsy-Anal Anomalies-Distal Phalangeal Hypoplasia
PUS3 Mutations Are Associated With Intellectual Disability, Leukoencephalopathy, and Nephropathy
Neurology: Genetics
Neurology
Genetics
