✦ LIBER ✦
IFR2BP2 Mutations Identified As a Novel Genetic Cause of Familial Common Variable Immunodeficiency Identified Via Support Vector Algorithm and Whole Exome Sequencing
✍ Scribed by Keller, Michael; Glessner, Joseph; Hakonarson, Hakon; Orange, Jordan
- Book ID
- 122893233
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 38 KB
- Volume
- 131
- Category
- Article
- ISSN
- 1097-6825
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