Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse-Reference-Cited by-同舟云学术

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Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

Published:2019-07-02 Issue:8 Volume:60 Page:2875
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Cross Sally H.¹,Mckie Lisa¹,Keighren Margaret¹,West Katrine¹,Thaung Caroline²³,Davey Tracey⁴,Soares Dinesh C.¹,Sanchez-Pulido Luis¹,Jackson Ian J.¹

Affiliation:

1. MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom

2. Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom

3. University College London Institute of Ophthalmology, London, United Kingdom

4. Electron Microscopy Research Services, Newcastle University, Newcastle, United Kingdom

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

Cited by 15 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. Nanophthalmos-Associated MYRF gene mutation facilitates intraocular inflammation in mice;International Immunopharmacology;2024-08

2. The Genetic Determinants of Axial Length: From Microphthalmia to High Myopia in Childhood;Annual Review of Genomics and Human Genetics;2023-08-25

3. Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse;Scientific Reports;2023-07-07

4. Comparative and longitudinal analysis of axial and retinal biometry in prospective models of hyperopia;2022-05-07

5. MYRF: A Mysterious Membrane-Bound Transcription Factor Involved in Myelin Development and Human Diseases;Neuroscience Bulletin;2021-04-17

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