Human Genome Epidemiology Literature Finder
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Query Trace: Vision and COL18A1[original query] |
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Knobloch syndrome caused by homozygous frameshift mutation of the COL18A1 gene in a Chinese pedigree. International journal of ophthalmology 2018 7 11 (6): 918-922. Zhang Lu-Si, Li Hai-Bo, Zeng Jun, Yang Yan, Ding Ch |
- Page last reviewed:Oct 1, 2023
- Page last updated:Nov 28, 2023
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