Ashraf Yahia

5PUBLICATIONS
29CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Te hītori ahurea Māori (Māori cultural history)
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Publications (5)

|Feb 05, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.

Mahmoud Koko, Maha A Elseed, Inaam N Mohammed

|Aug 01, 2023
Consanguinity and willingness to perform premarital genetic screening in Sudan.

Yasir Ahmed Mohammed Elhadi, Salma S Alrawa, Esraa S A Alfadul

|Apr 03, 2023
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations.

Ashraf Yahia, Ahlam A A Hamed, Inaam N Mohamed

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