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Prph2 disease mutations lead to structural and functional defects in the RPE.
Tebbe, Lars; Sakthivel, Haarthi; Makia, Mustafa S; Kakakhel, Mashal; Conley, Shannon M; Al-Ubaidi, Muayyad R; Naash, Muna I.
Affiliation
  • Tebbe L; Department of Biomedical Engineering, University of Houston, Houston, Texas, USA.
  • Sakthivel H; Department of Biomedical Engineering, University of Houston, Houston, Texas, USA.
  • Makia MS; Department of Biomedical Engineering, University of Houston, Houston, Texas, USA.
  • Kakakhel M; Department of Biomedical Engineering, University of Houston, Houston, Texas, USA.
  • Conley SM; Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA.
  • Al-Ubaidi MR; Department of Biomedical Engineering, University of Houston, Houston, Texas, USA.
  • Naash MI; Department of Biomedical Engineering, University of Houston, Houston, Texas, USA.
FASEB J ; 36(5): e22284, 2022 05.
Article in En | MEDLINE | ID: mdl-35344225
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinal Diseases / Tetraspanins / Peripherins Limits: Humans Language: En Journal: FASEB J Journal subject: BIOLOGIA / FISIOLOGIA Year: 2022 Type: Article Affiliation country: United States
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinal Diseases / Tetraspanins / Peripherins Limits: Humans Language: En Journal: FASEB J Journal subject: BIOLOGIA / FISIOLOGIA Year: 2022 Type: Article Affiliation country: United States