Human Genome Epidemiology Literature Finder
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Query Trace: Ophthalmoplegia and SEPN1[original query] |
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Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene. Neurology 2005 12 65 (12): 1930-5. Jungbluth H, Zhou H, Hartley L, Halliger-Keller B, Messina S, Longman C, Brockington M, Robb S A, Straub V, Voit T, Swash M, Ferreiro A, Bydder G, Sewry C A, Müller C, Muntoni |
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- Page last updated:Mar 25, 2024
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