ID   EMCi169-A
AC   CVCL_D0VD
SY   Clone_1
DR   BioSamples; SAMEA114004130
DR   hPSCreg; EMCi169-A
DR   Wikidata; Q123031234
RX   PubMed=37541189;
CC   From: Erasmus University Medical Center; Rotterdam; Netherlands.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_D0VE ! EMCi169-B
OI   CVCL_D0VF ! EMCi169-C
OI   CVCL_D0VG ! EMCi169-D
OI   CVCL_D0VH ! EMCi169-E
SX   Male
AG   Children
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 30-01-24; Version: 2
//
RX   PubMed=37541189; DOI=10.1016/j.ajhg.2023.07.005;
RA   Niggl E., Bouman A., Briere L.C., Hoogenboezem R.M., Wallaard I.,
RA   Park J., Admard J., Wilke M., Harris-Mostert E.D.R.O., Elgersma M.,
RA   Bain J., Balasubramanian M., Banka S., Benke P.J., Bertrand M.,
RA   Blesson A.E., Clayton-Smith J., Ellingford J.M., Gillentine M.A.,
RA   Goodloe D.H., Haack T.B., Jain M., Krantz I., Luu S.M., McPheron M.,
RA   Muss C.L., Raible S.E., Robin N.H., Spiller M., Starling S.,
RA   Sweetser D.A., Thiffault I., Vetrini F., Witt D., Woods E., Zhou D.-H.,
RA   Elgersma Y., van Esbroeck A.C.M.;
RT   "HNRNPC haploinsufficiency affects alternative splicing of
RT   intellectual disability-associated genes and causes a
RT   neurodevelopmental disorder.";
RL   Am. J. Hum. Genet. 110:1414-1435(2023).
//