The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource, 1 online resource.
- Sprache
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Englisch
- Erschienen in
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The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued ; volume:18 ; number:1 ; day:2 ; month:5 ; year:2023 ; pages:1-11 ; date:12.2023
Orphanet journal of rare diseases ; 18, Heft 1 (2.5.2023), 1-11, 12.2023
- Urheber
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Schröder, Simone
Yigit, Gökhan
Li, Yun
Altmüller, Janine
Büttel, Hans-Martin
Fiedler, Barbara
Kretzschmar, Christoph
Nürnberg, Peter
Seeger, Jürgen
Serpieri, Valentina
Valente, Enza Maria
Wollnik, Bernd
Boltshauser, Eugen
Brockmann, Knut
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s13023-023-02706-5
- URN
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urn:nbn:de:101:1-2023090511214798569111
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:58 MESZ
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Beteiligte
- Schröder, Simone
- Yigit, Gökhan
- Li, Yun
- Altmüller, Janine
- Büttel, Hans-Martin
- Fiedler, Barbara
- Kretzschmar, Christoph
- Nürnberg, Peter
- Seeger, Jürgen
- Serpieri, Valentina
- Valente, Enza Maria
- Wollnik, Bernd
- Boltshauser, Eugen
- Brockmann, Knut
- SpringerLink (Online service)
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