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Estimation of the Mutation Frequencies in Charcot-Marie-Tooth Disease Type 1 and Hereditary Neuropathy with Liability to Pressure Palsies: A European Collaborative Study
54 auth.
E. Nelis,
C. Broeckhoven,
P. Jonghe,
A. Löfgren,
A. Vandenberghe,
P. Latour,
É. Guern,
A. Brice,
M. Mostacciuolo,
F. Schiavon,
F. Palau,
S. Bort,
M. Upadhyaya,
M. Rocchi,
N. Archidiacono,
...
P. Mandich,
E. Bellone,
K. Silander,
M. Savontaus,
R. Navon,
H. Goldberg-Stern,
X. Estivill,
V. Volpini,
W. Friedl,
K. Zerres,
J. Tyson,
S. Malcolm,
B. Holmberg,
G. Holmgren,
E. Mariman,
A. Gabreëls-Festen,
C. Yapijakis,
D. Vassilopoulos,
C. Clark,
N. Haites,
P. Hilbert,
L. Maldergem,
B. Rautenstrauss,
H. Grehl,
R. Mountford,
K. Mann,
T. Bettecken,
J. Burgunder,
C. Hanemann,
H. Müller,
J. Hertz,
D. Schorderet,
T. Küntzer,
C. Wolf,
E. Kunert,
F. Muntoni,
P. Emmerick-Bock,
U. Orth,
A. Gal
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1996 |
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