C1QTNF5 missense variant causing autosomal dominant gyrate atrophy-like choroidal dystrophy.
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| Title: | C1QTNF5 missense variant causing autosomal dominant gyrate atrophy-like choroidal dystrophy. |
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| Authors: | Yang-Seeger, Denise1 (AUTHOR), Pauleikhoff, Laurenz J. B.1 (AUTHOR), Atiskova, Yevgeniya1 (AUTHOR), Thiele, Sarah1 (AUTHOR), Spitzer, Martin S.1 (AUTHOR), Birtel, Johannes1,2 (AUTHOR) study-enquiry@outlook.com |
| Source: | Ophthalmic Genetics. Aug2025, Vol. 46 Issue 4, p397-400. 4p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 187637796 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: C1QTNF5 missense variant causing autosomal dominant gyrate atrophy-like choroidal dystrophy. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Yang-Seeger%2C+Denise%22">Yang-Seeger, Denise</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pauleikhoff%2C+Laurenz+J%2E+B%2E%22">Pauleikhoff, Laurenz J. B.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Atiskova%2C+Yevgeniya%22">Atiskova, Yevgeniya</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Thiele%2C+Sarah%22">Thiele, Sarah</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Spitzer%2C+Martin+S%2E%22">Spitzer, Martin S.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Birtel%2C+Johannes%22">Birtel, Johannes</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> study-enquiry@outlook.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Ophthalmic+Genetics%22">Ophthalmic Genetics</searchLink>. Aug2025, Vol. 46 Issue 4, p397-400. 4p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=187637796 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1080/13816810.2025.2492037 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 4 StartPage: 397 Titles: – TitleFull: C1QTNF5 missense variant causing autosomal dominant gyrate atrophy-like choroidal dystrophy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Yang-Seeger, Denise – PersonEntity: Name: NameFull: Pauleikhoff, Laurenz J. B. – PersonEntity: Name: NameFull: Atiskova, Yevgeniya – PersonEntity: Name: NameFull: Thiele, Sarah – PersonEntity: Name: NameFull: Spitzer, Martin S. – PersonEntity: Name: NameFull: Birtel, Johannes IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: Aug2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 13816810 Numbering: – Type: volume Value: 46 – Type: issue Value: 4 Titles: – TitleFull: Ophthalmic Genetics Type: main |
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