G.O. 9 Dynamin 2 mutations are associated with dominant intermediate Charcot-Marie-Tooth disease and dominant centronuclear myopathy

2006 ◽  
Vol 16 (9-10) ◽  
pp. 725
Author(s):  
K.G. Claeys ◽  
S. Züchner ◽  
M. Kennerson ◽  
K. Verhoeven ◽  
C. Ceuterick ◽  
...  
Keyword(s):  
Centronuclear Myopathy ◽  
Charcot Marie Tooth ◽  
Charcot Marie Tooth Disease ◽  
Dynamin 2 ◽  
Tooth Disease

Mutations in the Pleckstrin Homology Domain of Dynamin 2 Cause Dominant Intermediate Charcot-Marie-Tooth Disease: LBS.002

Neurology ◽  
2005 ◽  
Vol 64 (10) ◽  
pp. 1826-1826 ◽  
Author(s):  
S. Zuchner ◽  
M. Noureddine ◽  
M. Kennerson ◽  
K. Verhoeven ◽  
K. Claeys ◽  
...  
Keyword(s):  
Pleckstrin Homology Domain ◽  
Pleckstrin Homology ◽  
Charcot Marie Tooth ◽  
Charcot Marie Tooth Disease ◽  
Dynamin 2 ◽  
Tooth Disease

Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease

Neurology ◽  
2007 ◽  
Vol 69 (3) ◽  
pp. 291-295 ◽  
Author(s):  
G. M. Fabrizi ◽  
M. Ferrarini ◽  
T. Cavallaro ◽  
I. Cabrini ◽  
R. Cerini ◽  
...  
Keyword(s):  
Novel Mutations ◽  
Charcot Marie Tooth ◽  
Charcot Marie Tooth Disease ◽  
Dynamin 2 ◽  
Tooth Disease

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

2005 ◽  
Vol 37 (3) ◽  
pp. 289-294 ◽  
Author(s):  
Stephan Züchner ◽  
Maher Noureddine ◽  
Marina Kennerson ◽  
Kristien Verhoeven ◽  
Kristl Claeys ◽  
...  
Keyword(s):  
Pleckstrin Homology Domain ◽  
Pleckstrin Homology ◽  
Charcot Marie Tooth ◽  
Charcot Marie Tooth Disease ◽  
Dynamin 2 ◽  
Tooth Disease
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