✦ LIBER ✦
De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy
✍ Scribed by H.J Durling; P Reilich; J Müller-Höcker; B Mendel; D Pongratz; C Wallgren-Pettersson; P Gunning; H Lochmüller; N.G Laing
- Book ID
- 117669664
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- English
- Weight
- 327 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0960-8966
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