✦ LIBER ✦
C.P.1.08 A homozygous deletion of TPM3 causing severe nemaline myopathy in two Turkish sib pairs from separate families
✍ Scribed by V. Lehtokari; K. Pelin; K. Donner; T. Voit; S. Rudnik-Schöneborn; C. Wallgren-Pettersson
- Book ID
- 116793102
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 48 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0960-8966
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