ID   HVRDi016-A
AC   CVCL_WS09
SY   PNN 1-38 (SMA); PNN1-38
DR   BioSamples; SAMEA12598003
DR   hPSCreg; HVRDi016-A
DR   Wikidata; Q94310009
RX   PubMed=28178525;
CC   From: Harvard University; Boston; USA.
DI   NCIt; C98670; Werdnig-Hoffmann disease
DI   ORDO; Orphanet_83330; Proximal spinal muscular atrophy type 1
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   1Y6M
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 21-03-23; Version: 5
//
RX   PubMed=28178525; DOI=10.1016/j.celrep.2017.01.035;
RA   Rodriguez-Muela N., Litterman N.K., Norabuena E.M., Mull J.L.,
RA   Galazo M.J., Sun C.-C., Ng S.-Y., Makhortova N.R., White A., Lynes M.M.,
RA   Chung W.K., Davidow L.S., Macklis J.D., Rubin L.L.;
RT   "Single-cell analysis of SMN reveals its broader role in neuromuscular
RT   disease.";
RL   Cell Rep. 18:1484-1498(2017).
//