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

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

Bibliographic Details
Main Authors:	Alireza Paniri, Sadegh Fattahi, Ahmad Rasoulinejad, Haleh Akhavan-Niaki
Format:	Article
Language:	English
Published:	Press of International Journal of Ophthalmology (IJO PRESS) 2021-04-01
Series:	International Journal of Ophthalmology
Online Access:	http://ies.ijo.cn/en_publish/2021/4/20210425.pdf

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