Comment on

• Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy.

  Donner K, Ollikainen M, Ridanpää M, Christen HJ, Goebel HH, de Visser M, Pelin K, Wallgren-Pettersson C. Donner K, et al. Neuromuscul Disord. 2002 Feb;12(2):151-8. doi: 10.1016/s0960-8966(01)00252-8. Neuromuscul Disord. 2002. PMID: 11738357
• Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2.

  Lehtokari VL, Ceuterick-de Groote C, de Jonghe P, Marttila M, Laing NG, Pelin K, Wallgren-Pettersson C. Lehtokari VL, et al. Neuromuscul Disord. 2007 Jun;17(6):433-42. doi: 10.1016/j.nmd.2007.02.015. Epub 2007 Apr 16. Neuromuscul Disord. 2007. PMID: 17434307