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A pathogenic DYT-THAP1 dystonia mutation causes hypomyelination and loss of YY1 binding.

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Title: A pathogenic DYT-THAP1 dystonia mutation causes hypomyelination and loss of YY1 binding.
Authors: Yellajoshyula D; Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA., Rogers AE; Molecular Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA., Kim AJ; Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA., Kim S; Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA.; Cellular and Molecular Biology Graduate Program, University of Michigan, Ann Arbor, MI 48109, USA., Pappas SS; Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.; Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA., Dauer WT; Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.; Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.; Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Source: Human molecular genetics [Hum Mol Genet] 2022 Mar 31; Vol. 31 (7), pp. 1096-1104.
Publication Type: Journal Article
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: A pathogenic DYT-THAP1 dystonia mutation causes hypomyelination and loss of YY1 binding.
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  Data: <searchLink fieldCode="AU" term="%22Yellajoshyula+D%22">Yellajoshyula D</searchLink>; Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Rogers+AE%22">Rogers AE</searchLink>; Molecular Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Kim+AJ%22">Kim AJ</searchLink>; Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.<br /><searchLink fieldCode="AU" term="%22Kim+S%22">Kim S</searchLink>; Department of Neurology, University of Michigan, Ann Arbor, MI 48109, USA.; Cellular and Molecular Biology Graduate Program, University of Michigan, Ann Arbor, MI 48109, USA.<br /><searchLink fieldCode="AU" term="%22Pappas+SS%22">Pappas SS</searchLink>; Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.; Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.<br /><searchLink fieldCode="AU" term="%22Dauer+WT%22">Dauer WT</searchLink>; Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.; Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.; Department of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2022 Mar 31; Vol. 31 (7), pp. 1096-1104.
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        Value: 10.1093/hmg/ddab310
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