A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: 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

Creator: Ibrahim, M. T.

Contributor: Alarcon-Martinez, T.
Lopez, I.
Fajardo, N.
Chiang, J.
Koenekoop, R. K.
SpringerLink (Online service)

DOI: 10.1038/s41598-018-22704-z

URN: urn:nbn:de:1111-201805201593

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 01.11.1151, 3:48 AM CET

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Ibrahim, M. T.
Alarcon-Martinez, T.
Lopez, I.
Fajardo, N.
Chiang, J.
Koenekoop, R. K.
SpringerLink (Online service)

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A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis

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Other Objects (12)

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