Resultats de la cerca - Nazha Birouk

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  1. 1
    A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3

    A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3 per Ahmed Bouhouche, Ali Benomar, Nazha Birouk, Angélique Mularoni, Farid Meggouh, Jean‐Pol Tassin, D. Grid, Antoon Vandenberghe, Mohamed Yahyaoui, T. Chkili, Alexis Brice, Eric LeGuern

    Publicat 1999
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  2. 2
    Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma

    Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated w... per Hamid Azzedine, Alessandra Bolino, T. Taïeb, Nazha Birouk, Marco Di Duca, Ahmed Bouhouche, Soufiène Benamou, A. Mrabet, T. Hammadouche, T. Chkili, Riadh Gouider, Roberto Ravazzolo, Alexis Brice, Jocelyn Laporte, Eric LeGuern

    Publicat 2003
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  3. 3
    Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

    Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia per Ziv Gan‐Or, Naïma Bouslam, Nazha Birouk, Alexandra Lissouba, Daniel B. Chambers, Julie Vérièpe, Alaura Androschuk, Sandra B. Laurent, Daniel Rochefort, Dan Spiegelman, Alexandre Dionne‐Laporte, Anna Szuto, Meijiang Liao, Denise A. Figlewicz, Ahmed Bouhouche, Ali Benomar, Mohamed Yahyaoui, Réda Ouazzani, Grace Yoon, Nicolas Dupré, Oksana Suchowersky, François V. Bolduc, J. Alex Parker, Patrick A. Dion, Pierre Drapeau, Guy A. Rouleau, Bouchra Ouled Amar Bencheikh

    Publicat 2016
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