Results
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3101.
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3102.
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3103.
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3104.
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3105.
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3106.
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3107.
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3108.
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3109.
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3110.
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3111.
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3112.
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Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies. [electronic resource] by
- Umehara, F
- Kiwaki, T
- Yoshikawa, H
- Nishimura, T
- Nakagawa, M
- Matsumoto, W
- Hashimoto, K
- Izumo, S
- Arimura, Y
- Arimura, K
Producer: 19960319
In:
Journal of the neurological sciences vol. 133
Availability: No items available.
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3113.
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Glycogen branching enzyme deficiency in adult polyglucosan body disease. [electronic resource] by
- Bruno, C
- Servidei, S
- Shanske, S
- Karpati, G
- Carpenter, S
- McKee, D
- Barohn, R J
- Hirano, M
- Rifai, Z
- DiMauro, S
Producer: 19930616
In:
Annals of neurology vol. 33
Availability: No items available.
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3114.
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3115.
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3116.
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3117.
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3118.
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3119.
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3120.
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