Ophthalmic Genetics
Volume 43, 2022 - Issue 5
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Research Report
A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family
Vanita Berrya Department of Genetics, UCL Institute of Ophthalmology, University College London, London, UK;b Moorfields Eye Hospital NHS Foundation Trust, London, UKCorrespondence[email protected]
https://orcid.org/0000-0001-6008-8970View further author information
Kaoru Fujinamia Department of Genetics, UCL Institute of Ophthalmology, University College London, London, UK;b Moorfields Eye Hospital NHS Foundation Trust, London, UK;c Laboratory of Visual Physiology, Division of Vision Research, National Institute of Sensory Organs, National Hospital Organization, Tokyo Medical Centre, Tokyo, Japan
https://orcid.org/0000-0003-4248-0033View further author information
Kiyofumi Mochizukid Department of Ophthalmology, Gifu University Graduate School of Medicine, Gifu, JapanView further author information
, Takeshi Iwatae Division of Molecular and Cellular Biology, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, JapanView further author information
, Nikolas Pontikosa Department of Genetics, UCL Institute of Ophthalmology, University College London, London, UK;b Moorfields Eye Hospital NHS Foundation Trust, London, UK
https://orcid.org/0000-0003-1782-4711View further author information
Roy A. Quinlanf Department of Biosciences, University of Durham, Durham, UKView further author information
& Michel Michaelidesa Department of Genetics, UCL Institute of Ophthalmology, University College London, London, UK;b Moorfields Eye Hospital NHS Foundation Trust, London, UKCorrespondence[email protected]
https://orcid.org/0000-0002-1552-7046View further author information
Pages 622-626
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Received 21 Apr 2022, Accepted 11 Jun 2022, Published online: 23 Jun 2022
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