Missense mutations in desmin associated with familial cardiac and skeletal myopathy
Nature Genetics1998Vol. 19(4), pp. 402–403
Citations Over TimeTop 10% of 1998 papers
Lev G. Goldfarb, Kyeyoon Park, Larisa Červen̆áková, Svetlana Gorokhova, Hee-Suk Lee, Olavo M. Vasconcelos, James W. Nagle, C. Semino–Mora, Kumaraswamy Sivakumar, Marinos C. Dalakas
Related Papers
- → Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations(2003)66 cited
- → Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene(2007)39 cited
- → Glucocorticoid treatment induces expression of small heat shock proteins in human satellite cell populations: consequences for a desmin-related myopathy involving the R120G alpha B-crystallin mutation(2002)24 cited
- DESMIN MYOPATHY, A SKELETAL MYOPATHY WITH CARDIOMYOPATHY CAUSED BY MUTATIONS IN THE DESMIN GENE(2000)
- → Desmin – related restrictive cardiomyopathy (RCD code: III-3E)(2013)