Novel mutations of the X-linked genes associated with early-onset high myopia in five Chinese families
Abstract Purpose To report novel pathogenic variants of X-linked genes in five Chinese families with early-onset high myopia (eoHM) by using whole-exome sequencing and analyzing the phenotypic features. Methods 5 probands with X-linked recessive related eoHM were collected in Ningxia Eye Hospital fr...
Saved in:
Main Authors: | Feiyin Zi (Author), Zhen Li (Author), Wanyu Cheng (Author), Xiaoyu Huang (Author), Xunlun Sheng (Author), Weining Rong (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2023-09-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia
by: Xiaoyu Huang, et al.
Published: (2023) -
De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
by: Xiaoyu Huang, et al.
Published: (2024) -
Effects of school myopia management measures on myopia onset and progression among Chinese primary school students
by: Jiao- jiao Shi, et al.
Published: (2023) -
Acute onset bilateral myopia induced by Chlordiazepoxide
by: Adel Hamid, et al.
Published: (2018) -
Acute onset bilateral myopia induced by Chlordiazepoxide
by: Adel Hamid, et al.
Published: (2018)