ID   UUIGPi002-A
SY   VHL3-9
DR   hPSCreg; UUIGPi002-A
RX   PubMed=31176917;
CC   From: Department of Immunology, Genetics and Pathology, Uppsala University; Uppsala; Sweden.
CC   Sequence variation: Heterozygous for VHL p.Ser65Leu (c.194C>T) (PubMed=31176917).
DI   NCIt; C3105; Von Hippel-Lindau syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Male
AG   37Y
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 05-07-19; Version: 1
RX   PubMed=31176917; DOI=10.1016/j.scr.2019.101474;
RA   Schuster J., Fatima A., Schwarz F., Klar J., Laan L., Dahl N.;
RT   "Generation of human induced pluripotent stem cell (iPSC) lines from
RT   three patients with von Hippel-Lindau syndrome carrying distinct VHL
RT   gene mutations.";
RL   Stem Cell Res. 38:101474-101474(2019).