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A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
Ghita Amalou
,
Crystel Bonnet
,
Zied Riahi
,
Aymane Bouzidi
,
Soukaina Elrharchi
,
et al.
Journal articles
pasteur-03215242v1
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Characterizing subcutaneous cortical auditory evoked potentials in mice
Olivier Postal
,
Warren Bakay
,
Typhaine Dupont
,
Alexa Buck
,
Christine Petit
,
et al.
Journal articles
hal-03852440v1
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Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
Soukaina Elrharchi
,
Zied Riahi
,
Sara Salime
,
Hicham Charoute
,
Lamiae Elkhattabi
,
et al.
Journal articles
pasteur-03219602v1
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Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness
Malak Salame
,
Crystel Bonnet
,
Ely Cheikh Mohamed Moctar
,
Selma Mohamed Brahim
,
Abdallahi Dedy
,
et al.
Journal articles
pasteur-04053511v1
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Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco
Imane Aitraise
,
Ghita Amalou
,
Amale Bousfiha
,
Hicham Charoute
,
Hassan Rouba
,
et al.
Journal articles
pasteur-03985530v1
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