✦ LIBER ✦
Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course
✍ Scribed by Luisa Sambati, Raffaele Agati, Antonella Bacci, Silvia Bianchi, Sabina Capellari
- Book ID
- 120966480
- Publisher
- Springer Milan
- Year
- 2012
- Tongue
- English
- Weight
- 306 KB
- Volume
- 34
- Category
- Article
- ISSN
- 1590-1874
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