Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human.

J Cell Mol Med · 2020 · PMC7412702 · PMID 32573113

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likely to be significantno p-value reported

We found that the alteration is likely to be significant because it causes structural instability to affect the cross‐linking or binding function of proteins.

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