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Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.

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Title: Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.
Authors: Casse, Fanny1 (AUTHOR), Courtin, Thomas1,2 (AUTHOR), Tesson, Christelle1 (AUTHOR), Ferrien, Mélanie1 (AUTHOR), Noël, Sandrine2 (AUTHOR), Fauret‐Amsellem, Anne‐Laure2 (AUTHOR), Gareau, Thomas1 (AUTHOR), Guegan, Justine1 (AUTHOR), Anheim, Mathieu3,4,5 (AUTHOR), Mariani, Louise‐Laure1,6 (AUTHOR), Le Forestier, Nadine6 (AUTHOR), Tranchant, Christine3,4,5 (AUTHOR), Corvol, Jean‐Christophe1,6 (AUTHOR), Lesage, Suzanne1 (AUTHOR), Brice, Alexis1 (AUTHOR) alexis.brice@icm-institute.org
Source: Movement Disorders Clinical Practice. Apr2023, Vol. 10 Issue 4, p664-669. 6p.
Database: Academic Search Ultimate
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  Data: Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.
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  Data: <searchLink fieldCode="JN" term="%22Movement+Disorders+Clinical+Practice%22">Movement Disorders Clinical Practice</searchLink>. Apr2023, Vol. 10 Issue 4, p664-669. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=163112623
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        Value: 10.1002/mdc3.13699
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      – Code: eng
        Text: English
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      – TitleFull: Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.
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              Text: Apr2023
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              Y: 2023
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