Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in <i>MTFMT</i>.

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作者： Dimitri M,Hemelsoet ^[1] ; Arnaud V,Vanlander ^[1] ; Joél,Smet ^[1] ; Elise,Vantroys ^[1] ; Marjan,Acou ^[1] ; Ingeborg,Goethals ^[1] ; Tom,Sante ^[1] ; Sara,Seneca ^[1] ; Bjorn,Menten ^[1] ; Rudy,Van Coster ^[1]

作者单位： Department of Neurology (D.M.H.), Ghent University Hospital; Department of Pediatrics (A.V.V., J.S., E.V., R.V.C.), Division of Pediatric Neurology and Metabolism, Ghent University Hospital; Department of Radiology (M.A.), Ghent University Hospital; Department of Nuclear Medicine (I.G.), Ghent University Hospital; Center for Medical Genetics Ghent (T.S., B.M.), Ghent University, Belgium; and Center for Medical Genetics (S.S.), UZ Brussel and Reproduction Genetics and Regenerative Medicine, Vrije Universiteit Brussel, Brussels, Belgium. ^[1]

DOI 10.1212/NXG.0000000000000298

PMID 30569017

发布时间 2022-03-30

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Neurology. Genetics

2018年4卷6期

e298页

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Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in <i>MTFMT</i>.

Neurology. Genetics

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Neurology. Genetics

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Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C&gt;T mutation in <i>MTFMT</i>.

Neurology. Genetics

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Neurology. Genetics

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Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in <i>MTFMT</i>.