✦ LIBER ✦
C.P.1.13 A homozygous null mutation in TPM2 gene causes autosomal recessive nemaline myopathy associated with multiple pterygia
✍ Scribed by P. Jouk; A. Labarre-Vila; P. Mezin; S. Drouhin; I. Marty; J. Lunardi; N. Monnier
- Book ID
- 116793107
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 64 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0960-8966
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