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Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa.
Zhang, Lin; Sun, Zixi; Zhao, Peiquan; Huang, Lulin; Xu, Mingchu; Yang, Yeming; Chen, Xue; Lu, Fang; Zhang, Xiang; Wang, Hui; Zhang, Shanshan; Liu, Wenjing; Jiang, Zhilin; Ma, Shi; Chen, Rui; Zhao, Chen; Yang, Zhenglin; Sui, Ruifang; Zhu, Xianjun.
Afiliación
  • Zhang L; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Sun Z; Center of Information in Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Zhao P; Department of Ophthalmology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
  • Huang L; Department of Ophthalmology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Xu M; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Yang Y; Department of Molecular and Human Genetics.
  • Chen X; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
  • Lu F; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Zhang X; Department of Ophthalmology, Hospital of Nanjing Medical University, State Key Laboratory of Reproductive Medicine, Nanjing, China.
  • Wang H; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Zhang S; Department of Ophthalmology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Liu W; Institute of Life Sciences, Hangzhou Normal University, Hangzhou, Zhejiang, China.
  • Jiang Z; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Ma S; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Chen R; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Zhao C; Institute of Laboratory Medicine, SichuanAcademy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, China.
  • Yang Z; Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
  • Sui R; Institute of Laboratory Medicine, SichuanAcademy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, China.
  • Zhu X; Department of Molecular and Human Genetics.
Hum Mol Genet ; 27(23): 4157-4168, 2018 12 01.
Article en En | MEDLINE | ID: mdl-30085091
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Degeneración Retiniana / Retinitis Pigmentosa / Hexoquinasa Tipo de estudio: Risk_factors_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: China
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Degeneración Retiniana / Retinitis Pigmentosa / Hexoquinasa Tipo de estudio: Risk_factors_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: China