Mutations in the β-tropomyosin (TMP2) gene in rare cases of autosomal dominant nemaline myopathy. - Donner,K.; Ollikainen,M.; Pelin,K.; Grönholm,M.; Carpén,O.; Wallgren-Pettersson,C.; Ridanpää,M. (Neuromuscul Disord, 2000)