TorsinA dysfunction causes persistent neuronal nuclear pore defects.

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Bibliographic Details
Title: TorsinA dysfunction causes persistent neuronal nuclear pore defects.
Authors: Pappas SS; Department of Neurology., Liang CC; Department of Neurology., Kim S; Cellular and Molecular Biology Program., Rivera CO; Department of Neurology., Dauer WT; Department of Neurology.; Cellular and Molecular Biology Program.; Department of Cell and Developmental Biology.; VA Ann Arbor Health System, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Source: Human molecular genetics [Hum Mol Genet] 2018 Feb 01; Vol. 27 (3), pp. 407-420.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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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ISSN:1460-2083
DOI:10.1093/hmg/ddx405