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Publications by Angham Abdulrahman Abdulkareem

Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and Intellectual Disability

Frontiers in Genetics

Molecular Medicine

English

A Novel Mutation in CACNA1A Gene in a Saudi Female With Episodic Ataxia Type 2 With No Response to Acetazolamide or 4-Aminopyridine

Intractable and Rare Diseases Research

English