Identification of a family with van der Hoeve's syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs.
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- Human Cell, 2024, v. 37, n. 3, p. 817, doi. 10.1007/s13577-024-01028-3
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- Article