ID   FMCPGHi003-A
AC   CVCL_D0F1
SY   301-iPSC-FHM-001A
DR   BioSamples; SAMEA115171192
DR   hPSCreg; FMCPGHi003-A
DR   Wikidata; Q123031296
RX   PubMed=38880015;
CC   From: The First Medical Center of PLA General Hospital; Beijing; China.
CC   Population: Chinese; Han.
CC   Sequence variation: Mutation; HGNC; HGNC:10585; SCN1A; Simple; p.Phe1774Cys (c.5321A>C); Zygosity=Heterozygous (PubMed=38880015).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C205634; Familial hemiplegic migraine-3
DI   ORDO; Orphanet_569; Familial or sporadic hemiplegic migraine
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   38Y
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 19-12-24; Version: 5
//
RX   PubMed=38880015; DOI=10.1016/j.scr.2024.103465;
RA   Wang T., Li Y.-N., Yang C.-X., Yuan H.-J., Na W.-N., Yu S.-Y.;
RT   "Generation of iPSC line (FMCPGHi003-A) from human PBMCs of a patient
RT   with familial hemiplegic migraine type 3.";
RL   Stem Cell Res. 79:103465-103465(2024).
//