B. Schlotter Weigel
AuthID: R-00F-ZKJ
1
TÃTULO: Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome Full Text
AUTORES: Rohkamm, B; Reilly, MM; Lochmuller, H; Schlotter Weigel, B; Barisic, N; Schols, L; Nicholson, G; Pareyson, D; Laura, M; Janecke, AR; Miltenberger Miltenyi, G; John, E; Fischer, C; Grill, F; Wakeling, W; Davis, M; Pieber, TR; Auer Grumbach, M;
PUBLICAÇÃO: 2007, FONTE: Journal of the Neurological Sciences, VOLUME: 263, NÚMERO: 1-2
AUTORES: Rohkamm, B; Reilly, MM; Lochmuller, H; Schlotter Weigel, B; Barisic, N; Schols, L; Nicholson, G; Pareyson, D; Laura, M; Janecke, AR; Miltenberger Miltenyi, G; John, E; Fischer, C; Grill, F; Wakeling, W; Davis, M; Pieber, TR; Auer Grumbach, M;
PUBLICAÇÃO: 2007, FONTE: Journal of the Neurological Sciences, VOLUME: 263, NÚMERO: 1-2
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