Tropomyosins in Skeletal Muscle Diseases
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-0-387-85766-4_12.pdf
Reference68 articles.
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3. Laing NG, Wilton SD, Akkari PA et al. A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy. Nat Genet 1995; 9:75–79.
4. Sung SS, Brassington AME, Grannatt K et al. Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes. Am J Hum Genet 2003; 72:681–690.
5. Lehtokari VL, Ceuterick-de Groote C, de Jonghe P et al. Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2. Neuromuscul Disord 2007; 17:433–442.
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