Autosomal Dominant Retinitis Pigmentosa Due to Class B <i>Rhodopsin</i> Mutations: An Objective Outcome for Future Treatment Trials.

Sumaroka, Alexander; Cideciyan, Artur V; Charng, Jason; Wu, Vivian; Powers, Christian A; Iyer, Bhavya S; Lisi, Brianna; Swider, Malgorzata; Jacobson, Samuel G

Autosomal Dominant Retinitis Pigmentosa Due to Class B Rhodopsin Mutations: An Objective Outcome for Future Treatment Trials.

Sumaroka, Alexander; Cideciyan, Artur V; Charng, Jason; Wu, Vivian; Powers, Christian A; Iyer, Bhavya S; Lisi, Brianna; Swider, Malgorzata; Jacobson, Samuel G.

Afiliação

Sumaroka A; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cideciyan AV; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Charng J; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Wu V; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Powers CA; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Iyer BS; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Lisi B; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Swider M; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Jacobson SG; Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Int J Mol Sci ; 20(21)2019 Oct 27.

Article em En | MEDLINE | ID: mdl-31717845

Assuntos

Mutação; Retinose Pigmentar/diagnóstico por imagem; Rodopsina/genética; Tomografia de Coerência Óptica/métodos; Adolescente; Adulto; Idoso; Idoso de 80 Anos ou mais; Estudos de Casos e Controles; Criança; Estudos Transversais; Feminino; Predisposição Genética para Doença; Humanos; Estudos Longitudinais; Masculino; Pessoa de Meia-Idade; Retinose Pigmentar/genética; Estudos Retrospectivos; Adulto Jovem

Palavras-chave

optical coherence tomography; photoreceptors; retinal degeneration; rods

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rodopsina / Retinose Pigmentar / Tomografia de Coerência Óptica / Mutação Tipo de estudo: Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

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