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Inaam N Mohamed

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Neurogenetics|July 27, 2024

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.

Parkinsonism & Related Disorders|June 21, 2022

Methylation of alpha-synuclein in a Sudanese cohortYousuf Bakhit, Ina Schmitt, Ahlam Hamed, et al.

European Journal of Human Genetics : EJHG|April 3, 2023

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerationsAshraf Yahia, Ahlam A A Hamed, Inaam N Mohamed, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Neurogenetics|July 27, 2024

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.

Parkinsonism & Related Disorders|June 21, 2022

Methylation of alpha-synuclein in a Sudanese cohortYousuf Bakhit, Ina Schmitt, Ahlam Hamed, et al.

European Journal of Human Genetics : EJHG|April 3, 2023

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerationsAshraf Yahia, Ahlam A A Hamed, Inaam N Mohamed, et al.

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