ID   ZIPi015-K
AC   CVCL_UD58
SY   AS_ID; ZIP15
DR   hPSCreg; ZIPi015-K
DR   Wikidata; Q98136517
RX   PubMed=30296670;
CC   From: Zentrum fur Integrative Psychiatrie; Kiel; Germany.
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75462; Angelman syndrome
DI   ORDO; Orphanet_72; Angelman syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_A8GQ ! ZIPi015-A
OI   CVCL_A8GR ! ZIPi015-B
OI   CVCL_A8GS ! ZIPi015-C
OI   CVCL_A8GT ! ZIPi015-D
OI   CVCL_A8GU ! ZIPi015-E
OI   CVCL_A8GV ! ZIPi015-F
OI   CVCL_A8GW ! ZIPi015-G
OI   CVCL_A8GX ! ZIPi015-H
OI   CVCL_A8GY ! ZIPi015-I
OI   CVCL_A8GZ ! ZIPi015-J
SX   Female
AG   12Y
CA   Induced pluripotent stem cell
DT   Created: 13-11-18; Last updated: 29-06-23; Version: 7
//
RX   PubMed=30296670; DOI=10.1016/j.scr.2018.09.015;
RA   Neureiter A., Brandl B., Hiber M., Tandon R., Muller F.-J.,
RA   Steenpass L.;
RT   "Generation of an iPSC line of a patient with Angelman syndrome due to
RT   an imprinting defect.";
RL   Stem Cell Res. 33:20-24(2018).
//