✦ LIBER ✦
Tay-Sachs disease in an Arab family due to c.78G>A HEXA nonsense mutation encoding a p.W26X early truncation enzyme peptide
✍ Scribed by Alireza Haghighi; Amira Masri; Ruth Kornreich; Robert J. Desnick
- Book ID
- 116989451
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 134 KB
- Volume
- 104
- Category
- Article
- ISSN
- 1096-7192
No coin nor oath required. For personal study only.