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Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy.
Peng, Yujiao; Zhao, Rulian; Dai, Erkuan; Peng, Li; He, Yunqi; Li, Shujin; Yang, Mu.
Afiliación
  • Peng Y; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, 12599University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Zhao R; Research Unit for Blindness Prevention of Chinese Academy of Medical Sciences (2019RU026), Sichuan Academy of Medical Sciences & 89669Sichuan Provincial People's Hospital, Chengdu, Sichuan, China.
  • Dai E; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, 12599University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Peng L; Research Unit for Blindness Prevention of Chinese Academy of Medical Sciences (2019RU026), Sichuan Academy of Medical Sciences & 89669Sichuan Provincial People's Hospital, Chengdu, Sichuan, China.
  • He Y; Ophthalmology, 91603Shanghai Jiaotong University School of Medicine Xinhua Hospital, Shanghai, China.
  • Li S; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, 12599University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Yang M; Research Unit for Blindness Prevention of Chinese Academy of Medical Sciences (2019RU026), Sichuan Academy of Medical Sciences & 89669Sichuan Provincial People's Hospital, Chengdu, Sichuan, China.
Eur J Ophthalmol ; 32(6): 3220-3226, 2022 Nov.
Article en En | MEDLINE | ID: mdl-35037517
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Enfermedades Hereditarias del Ojo / Oftalmopatías Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Eur J Ophthalmol Asunto de la revista: OFTALMOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades de la Retina / Enfermedades Hereditarias del Ojo / Oftalmopatías Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Eur J Ophthalmol Asunto de la revista: OFTALMOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: China