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RPE65 and retinal dystrophy: Report of new and recurrent mutations.
Safari, Shamsi; Zare-Abdollahi, Davood; Bushehri, Ata; Safari, Mohammad Reza; Dehghani, Azadeh; Tahmasebi, Zahra; Khorram Khorshid, Hamid Reza; Ghadami, Mohsen.
Affiliation
  • Safari S; Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
  • Zare-Abdollahi D; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Bushehri A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Safari MR; Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Dehghani A; Medical Biotechnology Research Center, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd, Iran.
  • Tahmasebi Z; Parseh Pathobiology and Genetics Center, Tehran, Iran.
  • Khorram Khorshid HR; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Ghadami M; Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
J Gene Med ; 22(3): e3154, 2020 03.
Article in En | MEDLINE | ID: mdl-31957135
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cis-trans-Isomerases / Retinal Pigment Epithelium / Leber Congenital Amaurosis / Retinal Dystrophies Limits: Female / Humans / Male Language: En Journal: J Gene Med Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Iran Country of publication: United kingdom
Fulltext
Add to My VHL
Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cis-trans-Isomerases / Retinal Pigment Epithelium / Leber Congenital Amaurosis / Retinal Dystrophies Limits: Female / Humans / Male Language: En Journal: J Gene Med Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Iran Country of publication: United kingdom