APA

Nouioua S., Hamadouche T., Funalot B., Bernard R., Bellatache N., Bouderba R., Grid D., Assami S., Benhassine T., Levy N., Vallat J. & Tazir M. (20120119). Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. : Neuromuscular disorders : NMD.

Chicago

Nouioua Sonia, Hamadouche Tarik, Funalot Benoit, Bernard Rafaëlle, Bellatache Nora, Bouderba Radia, Grid Djamel, Assami Salima, Benhassine Traki, Levy Nicolas, Vallat Jean-Michel and Tazir Meriem. 20120119. Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. : Neuromuscular disorders : NMD.

Harvard

Nouioua S., Hamadouche T., Funalot B., Bernard R., Bellatache N., Bouderba R., Grid D., Assami S., Benhassine T., Levy N., Vallat J. and Tazir M. (20120119). Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. : Neuromuscular disorders : NMD.

MLA

Nouioua Sonia, Hamadouche Tarik, Funalot Benoit, Bernard Rafaëlle, Bellatache Nora, Bouderba Radia, Grid Djamel, Assami Salima, Benhassine Traki, Levy Nicolas, Vallat Jean-Michel and Tazir Meriem. Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. : Neuromuscular disorders : NMD. 20120119.