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Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms.
Zheng, Yiqiao; Sun, Chi; Zhang, Xiaodong; Ruzycki, Philip A; Chen, Shiming.
Afiliación
  • Zheng Y; Molecular Genetic and Genomics Graduate Program, Division of Biological and Biomedical Sciences, Washington University in St Louis, Saint Louis, United States.
  • Sun C; Department of Ophthalmology and Visual Sciences, Washington University in St Louis, Saint Louis, United States.
  • Zhang X; Molecular Genetic and Genomics Graduate Program, Division of Biological and Biomedical Sciences, Washington University in St Louis, Saint Louis, United States.
  • Ruzycki PA; Department of Ophthalmology and Visual Sciences, Washington University in St Louis, Saint Louis, United States.
  • Chen S; Department of Ophthalmology and Visual Sciences, Washington University in St Louis, Saint Louis, United States.
Elife ; 122023 Nov 14.
Article en En | MEDLINE | ID: mdl-37963072
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Transactivadores Idioma: En Revista: Elife Año: 2023 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Transactivadores Idioma: En Revista: Elife Año: 2023 Tipo del documento: Article