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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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Description
ISSN:17501172
DOI:10.1186/s13023-023-02706-5