Various phenotypes of autosomal dominant cone-rod dystrophy with cone-rod homeobox mutation in two Chinese families.

Cui, Hui; Jin, Xin; Yang, Qing-Hua; Qu, Ling-Hui; Hou, Bao-Ke; Li, Zhao-Hui; Huang, Hou-Bin

Cui, Hui; Jin, Xin; Yang, Qing-Hua; Qu, Ling-Hui; Hou, Bao-Ke; Li, Zhao-Hui; Huang, Hou-Bin.

Afiliación

Cui H; Senior Department of Ophthalmology, the Third Medical Center of PLA General Hospital, Beijing 100853, China.
Jin X; Senior Department of Ophthalmology, the Third Medical Center of PLA General Hospital, Beijing 100853, China.
Yang QH; Senior Department of Ophthalmology, the Third Medical Center of PLA General Hospital, Beijing 100853, China.
Qu LH; Department of Ophthalmology, the 74th Army Group Hospital, Guangzhou 510318, Guangdong Province, China.
Hou BK; Senior Department of Ophthalmology, the Third Medical Center of PLA General Hospital, Beijing 100853, China.
Li ZH; Senior Department of Ophthalmology, the Third Medical Center of PLA General Hospital, Beijing 100853, China.
Huang HB; Senior Department of Ophthalmology, the Third Medical Center of PLA General Hospital, Beijing 100853, China.

Int J Ophthalmol ; 15(12): 1915-1923, 2022.

Article en En | MEDLINE | ID: mdl-36536961

Palabras clave

cone-rod dystrophy; cone-rod homeobox; mutation

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Int J Ophthalmol Año: 2022 Tipo del documento: Article País de afiliación: China

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