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PFIZi012-A

Donor information

Gender:Unknown

Disease status

Disease: chromosome 16p11.2 deletion syndrome, 220kb
Affected: Yes

General information

Depositor:Pfizer Limited - Pfizer
Cell line name:PFIZi012-A
Cell line alternative names:FB66c17, RCi198
Biosamples ID:SAMEA4097192
hPSCreg name:PFIZi012-A
This iPS cell line can only be used for research on Autism Spectrum Disorders or related neurodevelopmental disorders.