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Depot Institutionnel de l'UMBB >
Browsing by Author Hamadouche, Tarik
Showing results 6 to 8 of 8
Date de publication | Titre | Auteur(s) | 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 |
2010 | Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans | Lesage, Suzanne; Patin, Etienne; Condroyer, Christel; Leutenegger, Anne-Louise; Lohmann, Ebba; Giladi, Nir; Bar-Shira, Anat; Belarbi, Soraya; Hecham, Nassima; Pollak, Pierre; Ouvrard-Hernandez, Anne-Marie; Bardien, Soraya; Carr, Jonathan; Benhassine, Traki; Tomiyama, Hiroyuki; Pirkevi, Caroline; Hamadouche, Tarik; Cazeneuve, Cécile; Basak, A. Nazli; Hattori, Nobutaka; Dürr, Alexandra; Tazir, Meriem; Orr-Urtreger, Avi; Quintana-Murci, Lluis; Brice, Alexis |
2012 | Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H) | Baudot, Cécile; Esteve, Clothilde; Castro, Christel; Poitelon, Yannick; Mas, Camille; Hamadouche, Tarik; El-Rajab, Maryam; Lévy, Nicolas; Megarbané, André; Delague, Valérie |
Showing results 6 to 8 of 8
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