Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: MYOT[original query] |
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Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies. Orphanet journal of rare diseases 2014 9 121. Semmler Anna-Lena, Sacconi Sabrina, Bach J Elisa, Liebe Claus, Bürmann Jan, Kley Rudolf A, Ferbert Andreas, Anderheiden Roland, Van den Bergh Peter, Martin Jean-Jacques, De Jonghe Peter, Neuen-Jacob Eva, Müller Oliver, Deschauer Marcus, Bergmann Markus, Schröder J Michael, Vorgerd Matthias, Schulz Jörg B, Weis Joachim, Kress Wolfram, Claeys Kristl |
Rare variants in known and novel candidate genes predisposing to statin-associated myopathy. Pharmacogenomics 2016 Jun . Ne?oldová Magdaléna, Stránecký Viktor, Hoda?ová Kate?ina, Hartmannová Hana, Piherová Lenka, P?istoupilová Anna, Mrázová Lenka, Vrablík Michal, Adámková V?ra, Hubá?ek Jaroslav A, Jirsa Milan, Kmoch Stanisl |
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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