✦ LIBER ✦
CLN2/TPP1 deficiency: The novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype
✍ Scribed by C. Bessa; C.A. Teixeira; A. Dias; M. Alves; S. Rocha; L. Lacerda; L. Loureiro; A. Guimarães; M.G. Ribeiro
- Book ID
- 116988155
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 647 KB
- Volume
- 93
- Category
- Article
- ISSN
- 1096-7192
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