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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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