Author

Malik Ibrahim

Observed name: M. T. Ibrahim

Institution: University of Tripoli

Observed institutions: University of Tripoli, McGill University Health Centre, Research Institute of the McGill University Health Centre, McGill University

ORCID: 0009-0000-4495-7603

Observed ORCID: 0009-0000-4495-7603

OpenAlex ID: A5103797944

A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis

2018 · M. T. Ibrahim, T. Alarcon-Martinez, et al. · Scientific Reports · 34

Mucosal Phenotype as A Multidisciplinary Approach: A Narrative Review

2024 · Malik Ibrahim · Khalij-Libya Journal of Dental and Medical Research · 1

Works count: 2

Citation count: 35

H-index: 1

I10-index: 1