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X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations
Zahra Aadam
,
Nadia Kechout
,
Abdelhamid Barakat
,
Koon-Wing Chan
,
Meriem Ben-Ali
,
et al.
Journal articles
pasteur-01374987v1
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Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies
Aymane Bouzidi
,
Hicham Charoute
,
Majida Charif
,
Ghita Amalou
,
Mostafa Kandil
,
et al.
Journal articles
hal-03861095v1
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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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A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family
Sara Salime
,
Zied Riahi
,
Soukaina Elrharchi
,
Lamiae Elkhattabi
,
Hicham Charoute
,
et al.
Journal articles
pasteur-03219641v1
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A Novel Homozygous Missense Mutation in the FU-CRD2 Domain of the R-spondin1 Gene Associated with Familial 46,XX DSD
Yassine Naasse
,
Amina Bakhchane
,
Hicham Charoute
,
Farida Jennane
,
Joelle Bignon-Topalovic
,
et al.
Journal articles
pasteur-03521891v1
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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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Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.
Houda Benrahma
,
Hicham Charoute
,
Khaled Lasram
,
Redouane Boulouiz
,
Rym Kefi-Ben Atig
,
et al.
Journal articles
pasteur-01375062v1
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Association study of HNF1A polymorphisms with metabolic syndrome in the Moroccan population.
Imane Morjane
,
Rym Kefi
,
Hicham Charoute
,
Fouzia Lakbakbi El Yaagoubi
,
Meryem Hechmi
,
et al.
Journal articles
hal-01571303v1
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A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders
Amale Bousfiha
,
Amina Bakhchane
,
Hicham Charoute
,
Zied Riahi
,
Khalid Snoussi
,
et al.
Journal articles
pasteur-03219646v1
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Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness
Amale Bousfiha
,
Zied Riahi
,
Lamiae Elkhattabi
,
Amina Bakhchane
,
Hicham Charoute
,
et al.
Journal articles
pasteur-03219615v1
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Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population
Hicham Charoute
,
Rym Kefi
,
Safaa Bounaceur
,
Houda Benrahma
,
Ahmed Reguig
,
et al.
Journal articles
pasteur-01966344v1
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A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability
Al Mehdi Krami
,
Aymane Bouzidi
,
Majida Charif
,
Ghita Amalou
,
Hicham Charoute
,
et al.
Journal articles
hal-03861096v1
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