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Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations.
Zou, Gang; Zhang, Tao; Cheng, Xuesen; Igelman, Austin D; Wang, Jun; Qian, Xinye; Fu, Shangyi; Wang, Keqing; Koenekoop, Robert K; Fishman, Gerald A; Yang, Paul; Li, Yumei; Pennesi, Mark E; Chen, Rui.
Affiliation
  • Zou G; Department of Ophthalmology, Ningxia Eye Hospital, People's Hospital of Ningxia Hui Autonomous Region, First Affiliated Hospital of Northwest University for Nationalities, Ningxia Clinical Research Center on Diseases of Blindness in Eye, Yinchuan, China.
  • Zhang T; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Cheng X; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Igelman AD; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Wang J; Department of Ophthalmology, Casey Eye Institute, Oregon Health & Science University, Portland, Oregon.
  • Qian X; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Fu S; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Wang K; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Koenekoop RK; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Fishman GA; Department of Paediatric Surgery, Human Genetics and Adult Ophthalmology, MUHC, Montréal, Quebec, Canada.
  • Yang P; Pangere Center for Inherited Retinal Diseases, The Chicago Lighthouse, Chicago, IL.
  • Li Y; Department of Ophthalmology, Casey Eye Institute, Oregon Health & Science University, Portland, Oregon.
  • Pennesi ME; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas.
  • Chen R; Department of Ophthalmology, Casey Eye Institute, Oregon Health & Science University, Portland, Oregon.
Mol Vis ; 27: 95-106, 2021.
Article in En | MEDLINE | ID: mdl-33907365
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Full text: 1 Database: MEDLINE Main subject: Retinal Degeneration / RNA, Untranslated / Cytoskeletal Proteins / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Child, preschool / Female / Humans / Male Language: En Journal: Mol Vis Journal subject: BIOLOGIA MOLECULAR / OFTALMOLOGIA Year: 2021 Type: Article Affiliation country: China
Fulltext
Add to My VHL
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Full text: 1 Database: MEDLINE Main subject: Retinal Degeneration / RNA, Untranslated / Cytoskeletal Proteins / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Child, preschool / Female / Humans / Male Language: En Journal: Mol Vis Journal subject: BIOLOGIA MOLECULAR / OFTALMOLOGIA Year: 2021 Type: Article Affiliation country: China