A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Press of International Journal of Ophthalmology (IJO PRESS)
2021-04-01
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Series: | International Journal of Ophthalmology |
Online Access: | http://ies.ijo.cn/en_publish/2021/4/20210425.pdf |
ISSN: | 2222-3959 2227-4898 |
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