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Mutations of the slow muscle -tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

✍ Scribed by Wattanasirichaigoon, D.; Swoboda, K. J.; Takada, F.; Tong, H.-Q.; Lip, V.; Iannaccone, S. T.; Wallgren-Pettersson, C.; Laing, N. G.; Beggs, A. H.

Book ID: 119963751
Publisher: Lippincott Williams and Wilkins
Year: 2002
Tongue: English
Weight: 628 KB
Volume: 59
Category: Article
ISSN: 0028-3878
DOI: 10.1212/WNL.59.4.613

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