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Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32), peripheral myelin protein 22 (PMP22), and peripheral myelin protein zero (MPZ). [electronic resource] by
- Ekici, A B
- Schweitzer, D
- Park, O
- Lorek, D
- Rautenstrauss, B
- Krüger, G
- Friedl, W
- Uhlhaas, S
- Bathke, K
- Heuss, D
- Kayser, C
- Grehl, H
Producer: 20010222
In:
Neurogenetics vol. 3
Availability: No items available.
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