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Depot Institutionnel de l'UMBB >
Browsing by Author Nouioua, Sonia
Showing results 1 to 3 of 3
| Date de publication | Titre | Auteur(s) | | 2014 | Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases : an update | Tazir, Meriem; Hamadouche, Tarik; Nouioua, Sonia; Mathis, Stephane; Vallat, Jean-Michel |
| 2014 | Intragenic deletion patterns of dystrophin gene in duchenne and becker muscular dystrophy patients from algeria | Cherrallah, Amira; Benhassine, Traki; Nouioua, Sonia; MakriAffiliated, Samira; Chaouch, Malika; Tazir, Meriem; Hamadouche, Tarik |
| 2011 | Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes | Nouioua, Sonia; Hamadouche, Tarik; Funalot, Benoit; Bernard, Rafaëlle; Bellatache, Nora; Bouderba, Radia; Grid, Djamel; Assami, Salima; Benhassine, Traki; Levy, Nicolas; Vallat, Jean-Michel; Tazir, Meriem |
Showing results 1 to 3 of 3
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