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Publications by Evan Sticca

Mutations in MBOAT7 , Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features

American Journal of Human Genetics
Genetics
2016English

Related publications

Pachygyria-Intellectual Disability-Epilepsy Syndrome

2020English

X-Linked Spasticity-Intellectual Disability-Epilepsy Syndrome

2020English

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

American Journal of Human Genetics
Genetics
2012English

Concept Formation in a Child With an Intellectual Disability and Autistic Traits

The Japanese Journal of Special Education
1997English

Genetic and Neurodevelopmental Spectrum ofSYNGAP1-associated Intellectual Disability and Epilepsy

Journal of Medical Genetics
Genetics
2016English

Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability

American Journal of Human Genetics
Genetics
2014English

Perampanel and Challenging Behaviour in Intellectual Disability and Epilepsy: A Management Dilemma

Case Reports in Psychiatry
PsychiatryMental Health
2014English

Severe Intellectual Disability-Epilepsy-Anal Anomalies-Distal Phalangeal Hypoplasia

2020English

PUS3 Mutations Are Associated With Intellectual Disability, Leukoencephalopathy, and Nephropathy

Neurology: Genetics
NeurologyGenetics
2019English

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