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An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variant
✍ Scribed by Maria Teresa Dotti; Rosaria Buccoliero; Andrew Lee; J. Raphael Gorospe; Daniel Flint; Paolo Galluzzi; Silvia Bianchi; Camilla D’Eramo; Sakkubai Naidu; Antonio Federico; Michael Brenner
- Book ID
- 106094272
- Publisher
- Springer
- Year
- 2009
- Tongue
- English
- Weight
- 275 KB
- Volume
- 256
- Category
- Article
- ISSN
- 0340-5354
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