Clinical Phenotypes of <i>CDHR1</i>-Associated Retinal Dystrophies.

Malechka, Volha V; Cukras, Catherine A; Chew, Emily Y; Sergeev, Yuri V; Blain, Delphine; Jeffrey, Brett G; Ullah, Ehsan; Hufnagel, Robert B; Brooks, Brian P; Huryn, Laryssa A; Zein, Wadih M

Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies.

Malechka, Volha V; Cukras, Catherine A; Chew, Emily Y; Sergeev, Yuri V; Blain, Delphine; Jeffrey, Brett G; Ullah, Ehsan; Hufnagel, Robert B; Brooks, Brian P; Huryn, Laryssa A; Zein, Wadih M.

Afiliación

Malechka VV; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Cukras CA; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Chew EY; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Sergeev YV; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Blain D; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Jeffrey BG; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Ullah E; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Hufnagel RB; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Brooks BP; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Huryn LA; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Zein WM; Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Genes (Basel) ; 13(5)2022 05 22.

Article en En | MEDLINE | ID: mdl-35627310

Asunto(s)

Proteínas Relacionadas con las Cadherinas; Distrofias de Conos y Bastones; Proteínas del Tejido Nervioso; Distrofias Retinianas; Proteínas Relacionadas con las Cadherinas/genética; Cadherinas/genética; Distrofias de Conos y Bastones/genética; Electrorretinografía; Humanos; Mutación; Proteínas del Tejido Nervioso/genética; Fenotipo; Distrofias Retinianas/genética

Palabras clave

CDHR1; autosomal recessive retinal dystrophies; retinal dystrophy

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Distrofias Retinianas / Distrofias de Conos y Bastones / Proteínas Relacionadas con las Cadherinas / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

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