✦ LIBER ✦
Novel CLN3 mutation predicted to cause complete loss of protein function does not modify the classical JNCL phenotype
✍ Scribed by Jennifer M. Kwon; Paul G. Rothberg; Adam R. Leman; Jill M. Weimer; Jonathan W. Mink; David A. Pearce
- Book ID
- 116768006
- Publisher
- Elsevier Science
- Year
- 2005
- Tongue
- English
- Weight
- 92 KB
- Volume
- 387
- Category
- Article
- ISSN
- 0304-3940
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