检索结果 - Nazha Birouk

  • Showing 1 - 3 results of 3
Refine Results
  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 由 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

    出版 1999
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  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... 由 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

    出版 2003
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  3. 3
    Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

    Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia 由 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

    出版 2016
    获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: