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Sofiane Ouhab
Observed name:
S. Ouhab
OpenAlex ID:
A5065801473
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing
2015
·
Fatima Ammar‐Khodja
, Crystel Bonnet
, et al.
·
Molecular Genetics & Genomic Medicine
·
48
ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosis
2019
·
Malika Dahmani
, Sonia Talbi
, et al.
·
International Journal of Pediatric Otorhinolaryngology
·
7
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity
2025
·
Zied Riahi
, Sophie Boucher
, et al.
·
Proceedings of the National Academy of Sciences
·
1
PDF
Diversity of the genes involved in Algerian families with hearing loss identified by whole exome sequencing
2018
·
M. Dahmani
, F. Ammar Khodja
, et al.
·
New Biotechnology
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Works count:
4
Citation count:
56
H-index:
2
I10-index:
1
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