✦ LIBER ✦
2FC1.5 Exome sequencing and disease prediction implicate a mutation in KIF1A as a cause of hereditary spastic paraparesis type 30.
✍ Scribed by S. Edvardson; Y. Erlich; O. Elpeleg; E. Hodges; G. Hannon; T. Dor; A. Shaag
- Book ID
- 114360312
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 36 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1090-3798
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