A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations
| Main Authors: | , , , |
|---|---|
| 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 |