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The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. [electronic resource] by
- Eisenberg, I
- Avidan, N
- Potikha, T
- Hochner, H
- Chen, M
- Olender, T
- Barash, M
- Shemesh, M
- Sadeh, M
- Grabov-Nardini, G
- Shmilevich, I
- Friedmann, A
- Karpati, G
- Bradley, W G
- Baumbach, L
- Lancet, D
- Asher, E B
- Beckmann, J S
- Argov, Z
- Mitrani-Rosenbaum, S
Producer: 20010927
In:
Nature genetics vol. 29
Availability: No items available.
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