Autosomal dominant optic atrophy caused by six novel pathogenic OPA1 variants and genotype–phenotype correlation analysis

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Standort: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2415

Umfang: Online-Ressource

Sprache: Englisch

Anmerkungen: online resource.

Erschienen in: Autosomal dominant optic atrophy caused by six novel pathogenic OPA1 variants and genotype–phenotype correlation analysis ; volume:22 ; number:1 ; day:26 ; month:7 ; year:2022 ; pages:1-9 ; date:12.2022
BMC ophthalmology ; 22, Heft 1 (26.7.2022), 1-9, 12.2022

Urheber: Han, Jinfeng
Li, Ya
You, Ya
Fan, Ke
Lei, Bo

Beteiligte Personen und Organisationen: SpringerLink (Online service)

DOI: 10.1186/s12886-022-02546-0

URN: urn:nbn:de:101:1-2022100723070440289853

Rechteinformation: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Letzte Aktualisierung: 15.08.2025, 07:28 MESZ

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Beteiligte

Han, Jinfeng
Li, Ya
You, Ya
Fan, Ke
Lei, Bo
SpringerLink (Online service)

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Autosomal dominant optic atrophy caused by six novel pathogenic OPA1 variants and genotype–phenotype correlation analysis

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