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G.P.2 Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies
✍ Scribed by Cirak, S.; Foley, R.A.; Herrmann, R.; Willer, T.; Elisabeth, S.; Yau, M.; Brodd, L.; Torelli, S.; Kamynina, A.; Vondracek, P.; Roper, H.; Longman, C.; Korinthenberg, R.; Marrosu, G.; Nurnberg, P.; Plagnol, V.; Hurles, M.; Sewry, C.A.; Campbell, K.P.; Voit, T.; Muntoni, F.
- Book ID
- 119333663
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 52 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0960-8966
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