Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Myofibrillar Myopathy[original query] |
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Prevalence of desmin mutations in dilated cardiomyopathy. Circulation 2007 Mar 115 (10): 1244-51. Taylor Matthew R G, Slavov Dobromir, Ku Lisa, Di Lenarda Andrea, Sinagra Gianfranco, Carniel Elisa, Haubold Kurt, Boucek Mark M, Ferguson Debra, Graw Sharon L, Zhu Xiao, Cavanaugh Jean, Sucharov Carmen C, Long Carlin S, Bristow Michael R, Lavori Philip, Mestroni Luisa, , |
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis. Neuromuscular disorders : NMD 2015 Apr 25 (4): 289-96. Weihl Conrad C, Baloh Robert H, Lee Youjin, Chou Tsui-Fen, Pittman Sara K, Lopate Glenn, Allred Peggy, Jockel-Balsarotti Jennifer, Pestronk Alan, Harms Matthew |
Absence of myofibrillar myopathy in Quarter Horses with a histopathological diagnosis of type 2 polysaccharide storage myopathy and lack of association with commercial genetic tests. Equine veterinary journal 2022 3 55 (2): 230-238. Valberg Stephanie J, Henry Marisa L, Herrick Keely L, Velez-Irizarry Deborah, Finno Carrie J, Petersen Jessica |
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- Page last updated:Apr 29, 2024
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