ID   GM11269
AC   CVCL_4F12
DR   CLO; CLO_0025966
DR   Coriell; GM11269
DR   Wikidata; Q54844949
RX   PubMed=11738860;
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75488; Rett syndrome
DI   ORDO; Orphanet_778; Rett syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   13Y
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 7
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RX   PubMed=11738860; DOI=10.1016/S0387-7604(01)00339-4;
RA   Lee, Stephen Sung Jae
RA   Wan, Mi-Mi
RA   Francke, Uta
RT   "Spectrum of MECP2 mutations in Rett syndrome.";
RL   Brain Dev. 23 Suppl. 1:S138-S143(2001).
//