Mutations in the β-tropomyosin (TPM2) gene – a rare cause...

Neuromuscular Disorders 2002 Vol. 12; Iss. 2

Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

Kati Donner, Miina Ollikainen, Maaret Ridanpää, Hans-Jürgen Christen, Hans H Goebel, Marianne de Visser, Katarina Pelin, Carina Wallgren-Pettersson
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Volume:
12
Year:
2002
Language:
english
DOI:
10.1016/s0960-8966(01)00252-8
File:
PDF, 411 KB
english, 2002
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