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

✍ Scribed by Kati Donner; Miina Ollikainen; Maaret Ridanpää; Hans-Jürgen Christen; Hans H Goebel; Marianne de Visser; Katarina Pelin; Carina Wallgren-Pettersson

Book ID: 117669465
Publisher: Elsevier Science
Year: 2002
Tongue: English
Weight: 411 KB
Volume: 12
Category: Article
ISSN: 0960-8966
DOI: 10.1016/s0960-8966(01)00252-8

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