ID   LDS-iPSC8
AC   CVCL_DQ94
DR   Wikidata; Q54902394
RX   PubMed=27346194;
CC   From: Department of Dermatology, Jikei University School of Medicine; Tokyo; Japan.
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; HGNC:3801; FOXC2; Simple; c.724_727delCGCAinsAG; Zygosity=Unspecified (PubMed=27346194).
CC   Cell type: T-cell; CL=CL_0000084.
DI   NCIt; C128191; Lymphedema-distichiasis syndrome
DI   ORDO; Orphanet_33001; Lymphedema-distichiasis syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   18Y
CA   Induced pluripotent stem cell
DT   Created: 13-07-16; Last updated: 19-12-24; Version: 9
//
RX   PubMed=27346194; DOI=10.1016/j.scr.2016.03.004;
RA   Itoh M., Kawagoe S., Okano H.J., Nakagawa H.;
RT   "Integration-free T cell-derived human induced pluripotent stem cells
RT   (iPSCs) from a patient with lymphedema-distichiasis syndrome (LDS)
RT   carrying an insertion-deletion complex mutation in the FOXC2 gene.";
RL   Stem Cell Res. 16:611-613(2016).
//