BRCA2 c.156_157insAlu iPSC line (2041) cell line

Human iPSC disease model carrying the pathogenic BRCA2 c.156_157insAlu founder mutation associated with hereditary breast and ovarian cancer syndrome (HBOC). This model may be useful for studying BRCA2-associated hereditary cancer biology, DNA repair defects and early disease mechanisms in human-derived cellular systems.

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