A novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2415
- 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 novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy ; volume:22 ; number:1 ; day:16 ; month:12 ; year:2022 ; pages:1-11 ; date:12.2022
BMC ophthalmology ; 22, Heft 1 (16.12.2022), 1-11, 12.2022
- Urheber
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Haque, Obaid Imtiyazul
Chandrasekaran, Anbukayalvizhi
Nabi, Faisal
Ahmad, Owais
Marques, João Pedro
Ahmad, Tanweer
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s12886-022-02703-5
- URN
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urn:nbn:de:101:1-2023022721144463661713
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 14.08.2025, 10:46 MESZ
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Beteiligte
- Haque, Obaid Imtiyazul
- Chandrasekaran, Anbukayalvizhi
- Nabi, Faisal
- Ahmad, Owais
- Marques, João Pedro
- Ahmad, Tanweer
- SpringerLink (Online service)
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