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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 2 |
2004 | 1 |
2024 | 0 |
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Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.
N Engl J Med. 2000 Mar 16;342(11):770-80. doi: 10.1056/NEJM200003163421104.
N Engl J Med. 2000.
PMID: 10717012
Free article.
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
Park KY, Dalakas MC, Semino-Mora C, Lee HS, Litvak S, Takeda K, Ferrans VJ, Goldfarb LG.
Park KY, et al.
Clin Genet. 2000 Jun;57(6):423-9. doi: 10.1034/j.1399-0004.2000.570604.x.
Clin Genet. 2000.
PMID: 10905661
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A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin.
Dagvadorj A, Olivé M, Urtizberea JA, Halle M, Shatunov A, Bönnemann C, Park KY, Goebel HH, Ferrer I, Vicart P, Dalakas MC, Goldfarb LG.
Dagvadorj A, et al.
J Neurol. 2004 Feb;251(2):143-9. doi: 10.1007/s00415-004-0289-3.
J Neurol. 2004.
PMID: 14991347
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