Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genes.

Khateb, Samer; Shemesh, Aya; Offenheim, Ashly; Sheffer, Ruth; Ben-Yosef, Tamar; Chowers, Itay; Leibu, Rina; Baumann, Britta; Wissinger, Bernd; Kohl, Susanne; Banin, Eyal; Sharon, Dror

Khateb, Samer; Shemesh, Aya; Offenheim, Ashly; Sheffer, Ruth; Ben-Yosef, Tamar; Chowers, Itay; Leibu, Rina; Baumann, Britta; Wissinger, Bernd; Kohl, Susanne; Banin, Eyal; Sharon, Dror.

Afiliação

Khateb S; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.
Shemesh A; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.
Offenheim A; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.
Sheffer R; Department of Genetics, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.
Ben-Yosef T; Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Chowers I; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.
Leibu R; Department of Ophthalmology, Rambam Health Care Campus, Haifa, Israel.
Baumann B; Institute for Ophthalmic Research, Center for Ophthalmology, University of Tübingen, Tübingen, Germany.
Wissinger B; Institute for Ophthalmic Research, Center for Ophthalmology, University of Tübingen, Tübingen, Germany.
Kohl S; Institute for Ophthalmic Research, Center for Ophthalmology, University of Tübingen, Tübingen, Germany.
Banin E; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.
Sharon D; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.

Mol Vis ; 28: 21-28, 2022.

Article em En | MEDLINE | ID: mdl-35400991

Assuntos

Defeitos da Visão Cromática; Opsinas dos Cones; Miopia; Defeitos da Visão Cromática/genética; Opsinas dos Cones/genética; Eletrorretinografia; Haplótipos; Humanos; Miopia/genética; Linhagem; Fenótipo

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Defeitos da Visão Cromática / Opsinas dos Cones / Miopia Limite: Humans Idioma: En Revista: Mol Vis Assunto da revista: BIOLOGIA MOLECULAR / OFTALMOLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Israel

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