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Hassina Ibrahim
Hassina Ibrahim
Exome sequencing
Dominance (genetics)
Population
Genetics
Nonsyndromic deafness
2
Papers
45
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Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing
2015
Molecular Genetics & Genomic Medicine
Fatima Ammar-Khodja
Crystel Bonnet
Malika Dahmani
Sofiane Ouhab
Gaëlle Lefèvre
Hassina Ibrahim
Jean-Pierre Hardelin
Dominique Weil
Malek Louha
Christine Petit
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Citations (32)
EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss
2015
Orphanet Journal of Rare Diseases
Malika Dahmani
Fatima Ammar-Khodja
Crystel Bonnet
Gaelle M. Lefèvre
Jean-Pierre Hardelin
Hassina Ibrahim
Zahia Mallek
Christine Petit
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Citations (13)
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