IM
Inaam N. Mohammed

Publications (6)

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
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia
Article scientifique · 2021
Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family
Article scientifique · 2020
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family
Article scientifique · 2018
Research: Prevalence of neural tube defects Khartoum, Sudan August 2014–July 2015
Article scientifique · 2016

Domaines principaux

Sciences de la santé4 Sciences de la vie et biotechnologies2

Statistiques

Consultations24
Téléchargements0