Citations for
1MYOT, MYTP
Analysis of myotilin turnover provides mechanistic insight into the role of myotilinopathy-causing mutations.
von Nandelstadh P, Soliymani R, Baumann M, Carpen O.
Biochem J 436(1):113-21. 2011
2MYOT, MYTP
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.
Berciano J, Gallardo E, Domínguez-Perles R, Gallardo E, García A, García-Barredo R, Combarros O, Infante J, Illa I.
J Neurol Neurosurg Psychiatry 79(2):205-8. Epub 2007 Aug 13.PMID: 17698502 2008
3LGMD1A,MYOT,MYTP
Myotilinopathy: refining the clinical and myopathological phenotype.
Olive M, Goldfarb LG, Shatunov A, Fischer D, Ferrer I.
Brain 128(Pt 10):2315-26. Epub 2005 Jun 9. 2005
4 MYOT, LGMD1A, MYTP
Mutations in myotilin cause myofibrillar myopathy.
Selcen D, Engel AG.
Neurology 62(8):1363-71. Erratum in: Neurology. 2004 Jul 27;63(2):405. 2004