Inaam N Mohammed

Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan

O. Boespflug-Tanguy, M. Koko, S. Drunat, 2022, Frontiers in Genetics.

An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families

H. Lerche, G. Stevanin, P. Nürnberg, 2021, Annals of human genetics.

Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan

A. Durr, A. Brice, G. Stevanin, 2016, European Journal of Human Genetics.

Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.

J. Altmüller, M. Toliat, M. Koko, 2024, European journal of human genetics : EJHG.

Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia

F. Lamari, A. Brice, G. Stevanin, 2021, Frontiers in Neurology.

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal‐Recessive Juvenile‐Onset Parkinson's Disease

A. Durr, A. Brice, G. Stevanin, 2016, Annals of neurology.