Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract (Q44886976)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract |
scientific article |
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Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract (English)
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H Guo
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P Tong
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Y Peng
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T Wang
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Y Liu
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J Chen
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Y Li
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Q Tian
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Y Hu
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Y Zheng
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L Xiao
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W Xiong
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Q Pan
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Z Hu
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K Xia
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26 November 2013
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86
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6
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575-579
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