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.
Please note we may take up to three days to respond to your enquiry.
CancerTools.org uses the contact information provided to respond to you about our research tools and service. For more information please review our privacy policy.