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Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B. [electronic resource] by
- Kulkens, T
- Bolhuis, P A
- Wolterman, R A
- Kemp, S
- te Nijenhuis, S
- Valentijn, L J
- Hensels, G W
- Jennekens, F G
- de Visser, M
- Hoogendijk, J E
Producer: 19931209
In:
Nature genetics vol. 5
Availability: No items available.
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Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease. [electronic resource] by
- Gabreëls-Festen, A A
- Hoogendijk, J E
- Meijerink, P H
- Gabreëls, F J
- Bolhuis, P A
- van Beersum, S
- Kulkens, T
- Nelis, E
- Jennekens, F G
- de Visser, M
- van Engelen, B G
- Van Broeckhoven, C
- Mariman, E C
Producer: 19961122
In:
Neurology vol. 47
Availability: No items available.
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