Heba S. A. El

Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I

Ahmed Mosaeilhy, Magdy M. Mohamed, C. George Priya Doss et al. · Metabolic Brain Disease · 2017 · 47 citations

Genome-wide Association Study, Genotype-phenotype Association, Medicine +8

Two patients with Canavan disease and structural modeling of a novel mutation

Osama K. Zaki, Navaneethakrishnan Krishnamoorthy, Heba S. A. El et al. · Metabolic Brain Disease · 2016 · 38 citations

Novel Mutation, Allelic Variant, Genetic Disorder +9

Genotype–phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants

Osama K. Zaki, C. George Priya Doss, Salsabil A. Ali et al. · Human Molecular Genetics · 2017 · 38 citations · Full text

Phenotypic Variation, Genetics, Human Polymorphism +24

Novel mutation in an Egyptian patient with infantile Canavan disease

Osama K. Zaki, Heba S. A. El, Shaimaa A. Mohamed et al. · Metabolic Brain Disease · 2015 · 10 citations

Allergy, Genetic Disorder, Genetics +5