A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations

doi:10.18240/ijo.2021.04.25

Home > Archive>Volume 14, Issue 4, 2021 >636-638. DOI:10.18240/ijo.2021.04.25

A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations
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                        10.18240/ijo.2021.04.25
                    
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Corresponding Author:Haleh Akhavan-Niaki. Department of Genetics, Faculty of Medicine, Babol University of Medical Sciences, Babol 4717647745, Iran. halehakhavan@yahoo.com
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Alireza Paniri, Sadegh Fattahi, Ahmad Rasoulinejad, et al. A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations. Int J Ophthalmol, 2021,14(4):636-638

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Received:April 08,2020
Revised:July 15,2020
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Online: March 29,2021
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