Halima Nahili
Casablanca, Morocco
Last Updated: 09/26/2026
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Found 16 publications
Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: October 11, 2021
A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability.
Journal: European journal of medical genetics
Published: September 15, 2021
First characterization of congenital myasthenic syndrome type 5 in North Africa.
Journal: Molecular biology reports
Published: March 25, 2021
Association between G2677T/A polymorphism in ABCB1 gene and the risk of drug resistance epilepsy: An updated systematic review and meta-analysis.
Journal: Epilepsy research
Published: November 30, 2020
Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study.
Journal: BioMed research international
Published: April 29, 2020
First characterization of LHON pedigrees in North Africa.
Journal: Eye (London, England)
Published: December 06, 2019
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome.
Journal: International journal of pediatric otorhinolaryngology
Published: March 29, 2018
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.
Journal: Gene
Published: January 01, 2018
Methylenetetrahydrofolate Reductase Gene Polymorphisms (C677T and A1298C) and Hemorrhagic Stroke in Moroccan Patients.
Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
Published: September 28, 2017
Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees.
Journal: PloS one
Published: May 08, 2015
Last Updated: 09/26/2026