Human Genome Epidemiology Literature Finder
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Query Trace: Ophthalmoplegia and SPG7[original query] |
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A founder mutation p.H701P identified as a major cause of SPG7 in Norway. European journal of neurology 2016 Jan . Rydning S L, Wedding I M, Koht J, Chawla M, Øye A-M, Sheng Y, Vigeland M D, Selmer K K, Tallaksen C M |
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- Page last updated:Apr 16, 2024
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