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FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation. [electronic resource] by
- Sperfeld, A D
- Collatz, M B
- Baier, H
- Palmbach, M
- Storch, A
- Schwarz, J
- Tatsch, K
- Reske, S
- Joosse, M
- Heutink, P
- Ludolph, A C
Producer: 19991124
In:
Annals of neurology vol. 46
Availability: No items available.
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Long-term MRI and clinical follow-up of symptomatic and presymptomatic carriers of dysferlin gene mutations. [electronic resource] by
- Brummer, D
- Walter, M C
- Palmbach, M
- Knirsch, U
- Karitzky, J
- Tomczak, R
- Braun, C
- Grundhoff, N
- Bornemann, A
- Müller, C R
- Lochmüller, H
- Schreiber, H
Producer: 20060127
In:
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology vol. 24
Availability: No items available.
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