EE
Esraa Eltaraifee

Publications (3)

Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degeneration
Article scientifique · 2022
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
Article scientifique · 2022
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan
Article scientifique · 2022

Domaines principaux

Sciences de la santé2 Sciences de la vie et biotechnologies1

Statistiques

Consultations15
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