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ArticleBMC medical genomics2023

Novel compound heterozygous variants of the SEC23A gene in a Chinese family with cranio-lenticulo-sutural dysplasia based on data from a large cohort of congenital cataract patients.

Qiwei Wang et al.PubMed ↗Full text ↗Publisher ↗

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2023
2024
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Full record →Abstract, authors, funding and every citing paper · PMID 37828500