Your browser doesn't support javascript.
loading
PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY.
Zou, Xuan; Fu, Qing; Fang, Sha; Li, Hui; Ge, Zhongqi; Yang, Lizhu; Xu, Mingchu; Sun, Zixi; Li, Huajin; Li, Yumei; Dong, Fangtian; Chen, Rui; Sui, Ruifang.
Afiliación
  • Zou X; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Fu Q; Department of Ophthalmology, Huashan Hospital, Fudan University, Shanghai, China.
  • Fang S; School of Statistics, Capital University of Economics and Business, Beijing, China.
  • Li H; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Ge Z; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Yang L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Xu M; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Sun Z; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Li H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Li Y; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Dong F; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Chen R; Department of Ophthalmology, Huashan Hospital, Fudan University, Shanghai, China.
  • Sui R; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
Retina ; 39(10): 2040-2052, 2019 Oct.
Article en En | MEDLINE | ID: mdl-30134391
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Agudeza Visual / Enfermedades Hereditarias del Ojo / Oxidorreductasas de Alcohol / Distrofias Retinianas / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Retina Año: 2019 Tipo del documento: Article País de afiliación: China
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Agudeza Visual / Enfermedades Hereditarias del Ojo / Oxidorreductasas de Alcohol / Distrofias Retinianas / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Retina Año: 2019 Tipo del documento: Article País de afiliación: China