Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK) von Bousfiha, A., Bakhchane, A., Elrharchi, S., Dehbi, H., Kabine, M., Nadifi, S., Charoute, H., Barakat, A.

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A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family von Amalou, Ghita, Bonnet, Crystel, Riahi, Zied, Bouzidi, Aymane, Elrharchi, Soukaina, Bousfiha, Amale, Charif, Majida, Kandil, Mostafa, Lenaers, Guy, Petit, Christine, Barakat, Abdelhamid

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Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family von Elrharchi, Soukaina, Riahi, Zied, Salime, Sara, Charoute, Hicham, Elkhattabi, Lamiae, Boulouiz, Redouane, Kabine, Mostafa, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid

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Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families von Salime, Sara, Charif, Majida, Bousfiha, Amale, Elrharchi, Soukaina, Bakhchane, Amina, Charoute, Hicham, Kabine, Mostafa, Snoussi, Khalid, Lenaers, Guy, Barakat, Abdelhamid

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A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family von Salime, Sara, Riahi, Zied, Elrharchi, Soukaina, Elkhattabi, Lamiae, Charoute, Hicham, Nahili, Halima, Rouba, Hassan, Kabine, Mostafa, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid

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Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome von Elrharchi, Soukaina, Riahi, Zied, Salime, Sara, Nahili, Halima, Rouba, Hassan, Kabine, Mostafa, Bonnet, Crystel, Petit, Christine, Barakat, Abdelhamid

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