✦ LIBER ✦
P.9.6 Combined cap disease and nemaline myopathy in the same patient caused by an autosomal dominant mutation in the TPM3 gene
✍ Scribed by Malfatti, E.; Schaeffer, U.; Chapon, F.; Yang, Y.; Eymard, B.; Xu, R.; Laporte, J.; Romero, N.B.
- Book ID
- 123353316
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 46 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0960-8966
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