Amina Bakhchane
Casablanca, 20360, Morocco
Last Updated: 09/26/2026
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Found 24 publications
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 08, 2025
Genetic diversity of Usher syndrome in Moroccan patients.
Journal: Human genetics
Published: November 20, 2024
Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1.
Journal: Immunobiology
Published: July 21, 2020
Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness.
Journal: Human heredity
Published: July 02, 2019
A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD.
Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Published: October 30, 2017
Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile.
Journal: BMC research notes
Published: June 15, 2017
Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.
Journal: International journal of pediatric otorhinolaryngology
Published: March 21, 2017
Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population.
Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population.
Journal: Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis
Published: October 13, 2016
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.
Journal: Human genome variation
Published: July 15, 2016
Last Updated: 09/26/2026