A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis ; volume:8 ; number:1 ; day:22 ; month:3 ; year:2018 ; pages:1-6 ; date:12.2018
Scientific reports ; 8, Heft 1 (22.3.2018), 1-6, 12.2018
- Urheber
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Ibrahim, M. T.
- Beteiligte Personen und Organisationen
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Alarcon-Martinez, T.
Lopez, I.
Fajardo, N.
Chiang, J.
Koenekoop, R. K.
SpringerLink (Online service)
- DOI
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10.1038/s41598-018-22704-z
- URN
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urn:nbn:de:1111-201805201593
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:48 MESZ
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Beteiligte
- Ibrahim, M. T.
- Alarcon-Martinez, T.
- Lopez, I.
- Fajardo, N.
- Chiang, J.
- Koenekoop, R. K.
- SpringerLink (Online service)
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