ID   WG2324
AC   CVCL_B3YP
DR   Wikidata; Q110434110
RX   CelloPub=CLPUB00669;
RX   PubMed=27233228;
RX   PubMed=31462756;
CC   From: Montreal Children's Hospital cell repository; Montreal; Canada.
CC   Population: Caucasian.
CC   Omics: Genomics; Whole genome sequencing.
CC   Omics: Transcriptomics; RNAseq.
CC   Miscellaneous: Cell line no longer available.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C98986; Methylmalonic acidemia
DI   ORDO; Orphanet_293355; Methylmalonic acidemia without homocystinuria
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   13Y
CA   Finite cell line
DT   Created: 16-12-21; Last updated: 10-04-25; Version: 5
//
RX   CelloPub=CLPUB00669;
RA   Chu J.;
RT   "Investigation of patients diagnosed with mut methylmalonic aciduria.";
RL   Thesis MSc (2017); McGill University Montreal; Montreal; Canada.
//
RX   PubMed=27233228; DOI=10.1016/j.ymgme.2016.05.014;
RA   Chu J., Pupavac M., Watkins D., Tian X., Feng Y.-M., Chen S., Fenter R.,
RA   Zhang V.W., Wang J., Wong L.-J., Rosenblatt D.S.;
RT   "Next generation sequencing of patients with mut methylmalonic
RT   aciduria: validation of somatic cell studies and identification of 16
RT   novel mutations.";
RL   Mol. Genet. Metab. 118:264-271(2016).
//
RX   PubMed=31462756; DOI=10.1038/s41436-019-0640-9;
RA   Abdrabo L.S., Watkins D., Wang S.R., Lafond-Lapalme J., Riviere J.-B.,
RA   Rosenblatt D.S.;
RT   "Genome and RNA sequencing in patients with methylmalonic aciduria of
RT   unknown cause.";
RL   Genet. Med. 22:432-436(2020).
//