ID WC005i-FX11-7 AC CVCL_EJ76 SY FX11-7 DR WiCell; wc005i-fx11-7 DR Wikidata; Q54993616 RX PubMed=24654675; CC Sequence variation: Mutation; HGNC; HGNC:3775; FMR1; Repeat_expansion; CGG[>435]; ClinVar=VCV000009972; Zygosity=Hemizygous (PubMed=24654675). CC Derived from site: In situ; Skin; UBERON=UBERON_0002097. CC Cell type: Fibroblast of skin; CL=CL_0002620. DI NCIt; C84717; Fragile X syndrome DI ORDO; Orphanet_908; Fragile X syndrome OX NCBI_TaxID=9606; ! Homo sapiens (Human) OI CVCL_EJ77 ! WC006i-FX11-9U SX Male AG 7Y CA Induced pluripotent stem cell DT Created: 26-09-16; Last updated: 19-12-24; Version: 13 // RX PubMed=24654675; DOI=10.1089/scd.2014.0030; PMCID=PMC4103262; RA Doers M.E., Musser M.T., Nichol R., Berndt E.R., Baker M., Gomez T.M., RA Zhang S.-C., Abbeduto L., Bhattacharyya A.; RT "iPSC-derived forebrain neurons from FXS individuals show defects in RT initial neurite outgrowth."; RL Stem Cells Dev. 23:1777-1787(2014). //