✦ LIBER ✦
G.O.1 The phenotype of myofibrillar myopathy associated with p.W2710X mutation in filamin C: A study of 31 German patients
✍ Scribed by R.A. Kley; J. Kirschner; K. Eger; D. Fischer; A. Huebner; M. Vorgerd
- Book ID
- 116793429
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 47 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0960-8966
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