DOI:
10.1055/s-00000041
Neuropediatrics
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References
Donner K, Ollikainen M, Ridanpää M. , et al.
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy.
Neuromuscul Disord 2002;
12 (02) 151-158
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