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The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued.

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Title: The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued.
Authors: Schröder, Simone1 (AUTHOR), Yigit, Gökhan2 (AUTHOR), Li, Yun2 (AUTHOR), Altmüller, Janine3,4,5 (AUTHOR), Büttel, Hans-Martin6 (AUTHOR), Fiedler, Barbara7 (AUTHOR), Kretzschmar, Christoph8 (AUTHOR), Nürnberg, Peter3 (AUTHOR), Seeger, Jürgen9 (AUTHOR), Serpieri, Valentina10 (AUTHOR), Valente, Enza Maria10,11 (AUTHOR), Wollnik, Bernd2,12 (AUTHOR), Boltshauser, Eugen13 (AUTHOR), Brockmann, Knut1 (AUTHOR) kbrock@med.uni-goettingen.de
Source: Orphanet Journal of Rare Diseases. 5/2/2023, Vol. 18 Issue 1, p1-11. 11p.
Database: Academic Search Ultimate
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An: 163449239
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  Data: The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued.
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 5/2/2023, Vol. 18 Issue 1, p1-11. 11p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=163449239
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        Value: 10.1186/s13023-023-02706-5
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      – Code: eng
        Text: English
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      – TitleFull: The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued.
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              Text: 5/2/2023
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              Y: 2023
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