Barely Significant
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<i>ITGB5</i> mutation discovered in a Chinese family with blepharophimosis-ptosis-epicanthus inversus syndrome.

Open Life Sci · 2021 · PMC8665901 · PMID 34966851

1
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showed a trendno p-value reported
Both male and female family members had the disease, which was in line with an autosomal-dominant inheritance pattern, and the disease showed a trend of aggravation by generation.

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