Najoua Miladi
Tunis, Tunisia
Last Updated: 09/26/2026
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Found 8 publications
Using Exome Sequencing to Identify the Causes of Neurodevelopmental Disorders: Experience of a North African Genetic Center.
Journal: Clinical genetics
Published: December 22, 2025
Cracking the Code: Genotype-Phenotype Correlation Models in Sarcoglycanopathies.
Journal: Annals of clinical and translational neurology
Published: November 21, 2025
Novel missense variants in CFL2 affect F-actin depolymerisation and expand the disease spectrum of CFL2-related myopathy.
Journal: Human molecular genetics
Published: March 14, 2025
Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review.
Journal: Molecular cytogenetics
Published: August 01, 2022
Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: July 24, 2015
Association study of mitochondrial DNA polymorphisms with type 2 diabetes in Tunisian population.
Journal: Mitochondrial DNA
Published: October 10, 2013
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Last Updated: 09/26/2026