CRISPR correction of the Finnish ornithine delta-aminotransferase mutation restores metabolic homeostasis in iPSC from patients with gyrate atrophy-Reference-Cited by-同舟云学术

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CRISPR correction of the Finnish ornithine delta-aminotransferase mutation restores metabolic homeostasis in iPSC from patients with gyrate atrophy

Published:2022-06 Issue: Volume:31 Page:100863
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Maldonado Rocio,Jalil Sami,Keskinen Timo,Nieminen Anni I.,Hyvönen Mervi E.,Lapatto Risto,Wartiovaara Kirmo

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference32 articles.

1. The natural history of gyrate atrophy of the choroid and retina;Takki;Ophthalmology,1981

2. Cataract in gyrate atrophy: Clinical and morphologic studies;Kaiser-Kupfer;Investig. Ophthalmol. Vis. Sci.,1983

3. Gyrate atrophy of the choroid and retina with hyperornithinemia: Tubular aggregates and type 2 fiber atrophy in muscle;Sipila;Neurology,1979

4. Muscle creatine phosphate in gyrate atrophy of the choroid and retina with hyperornithinaemia - clues to pathogenesis;Heinänen;Eur. J. Clin. Investig.,1999

5. Raised plasma-ornithine and gyrate atrophy of the choroid and retina;Simell;Lancet,1973

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Induced Pluripotent Stem Cells and CRISPR-Cas9 Innovations for Treating Alpha-1 Antitrypsin Deficiency and Glycogen Storage Diseases;Cells;2024-06-18

2. Girate atrophy: clinical and functional features;Russian Pediatric Ophthalmology;2023-07-28

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