SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia (Q24298661)

GOA release 2020-03-11

BMP signaling pathway

1 reference

GOA release 2020-03-11

1 reference

Hui Guo

1

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Xuemin Jin

2

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Tengfei Zhu

3

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Tianyun Wang

4

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Ping Tong

5

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Lei Tian

6

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Yu Peng

7

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Liangdan Sun

8

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Anran Wan

9

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Jingjing Chen

10

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Yanling Liu

11

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Ying Li

12

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Qi Tian

13

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Lu Xia

14

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Lusi Zhang

15

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Yongcheng Pan

16

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Lina Lu

17

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Qiong Liu

18

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Lu Shen

19

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Yunping Li

20

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Wei Xiong

21

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Jiada Li

22

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Beisha Tang

23

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Yong Feng

24

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Xuejun Zhang

25

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Zhuohua Zhang

26

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Qian Pan

27

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Zhengmao Hu

28

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Kun Xia

Journal of Medical Genetics

29

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language of work or name

English

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publication date

August 2014

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published in

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volume

51

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issue

8

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page(s)

518-25

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cites work

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High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2

27 September 2017

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Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome--an autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13

27 September 2017

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Retinal and choroidal TGF-beta in the tree shrew model of myopia: isoform expression, activation and effects on function

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Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract

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Identifiers

DOI

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1658724

1658724

1 reference

1 reference

1 reference