Mohammad M. Kabiraj

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Christelle Tesson, Magdalena Nawara, Mustafa A. Salih et al. · The American Journal of Human Genetics · 2012 · 196 citations · Full text

Metabolic Syndrome, Energy Metabolism, Metabolic Disorder +9

Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes

Violeta Mihaylova, Juliane S. Müller, Juan J. Vílchez et al. · Brain · 2008 · 159 citations · Full text

Developmental Anomaly, Rare Diseases, Ache Deficiency +13

<i>SLC25A22</i>is a novel gene for migrating partial seizures in infancy

Annapurna Poduri, Erin L. Heinzen, Vida Chitsazzadeh et al. · Annals of Neurology · 2013 · 114 citations · Full text

Rundataxin, a novel protein with RUN and diacylglycerol binding domains, is mutant in a new recessive ataxia

Mirna Assoum, Mustafa A. Salih, Nathalie Drouot et al. · Brain · 2010 · 54 citations · Full text

Genetics, Molecular Biology, Molecular Genetics +16

New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations

Mustafa A. Salih, Emeline Mundwiller, Arif O. Khan et al. · PLoS ONE · 2013 · 52 citations · Full text

Genetics, Molecular Biology, Brain Iron Accumulation +18