Maladie de Charcot-Marie-Tooth associée au gène de la périaxine (CMT4F) : description clinique, électrophysiologique et génétique de 24 patients-Reference-Cited by-同舟云学术

Maladie de Charcot-Marie-Tooth associée au gène de la périaxine (CMT4F) : description clinique, électrophysiologique et génétique de 24 patients

Published:2013-08 Issue:8-9 Volume:169 Page:603-612
ISSN:0035-3787
Container-title:Revue Neurologique
language:fr
Short-container-title:Revue Neurologique

Author:

Renouil M.,Stojkovic T.,Jacquemont M.L.,Lauret K.,Boué P.,Fourmaintraux A.,Randrianaivo H.,Tallot M.,Mignard D.,Roelens P.,Tabailloux D.,Bernard R.,Cartault F.,Chane-Thien E.,Dubourg O.,Ferrer X.,Sole G.,Fournier E.,Latour P.,Lacour A.,Mignard C.

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

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3. Charcot-Marie-Tooth. Neuropathy Type 4;Bird,1993

4. Periaxin mutations cause recessive Dejerine-Sottasneuropathy;Boerkoel;Am J Hum Genet,2001

5. Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2;Bolino;Nat Genet,2000

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