ID   GIS2014-WT4C10
AC   CVCL_QX38
DR   Wikidata; Q54835843
RX   PubMed=28395737;
CC   Sequence variation: Mutation; HGNC; HGNC:644; AR; Repeat_expansion; (CAG)24 (c.172_174CAG(10_36)); ClinVar=VCV000009818; Zygosity=Hemizygous (PubMed=28395737).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
ST   Source(s): PubMed=28395737
ST   Amelogenin: X,Y
ST   CSF1PO: 10,11
ST   D10S1248: 14,15
ST   D12S391: 17,20
ST   D13S317: 11,12
ST   D16S539: 13
ST   D18S51: 14,15
ST   D19S433: 16
ST   D1S1656: 11,16
ST   D21S11: 28,32.2
ST   D22S1045: 11,17
ST   D2S1338: 19,25
ST   D2S441: 11,14
ST   D3S1358: 16,18
ST   D5S818: 11,12
ST   D7S820: 9,12
ST   D8S1179: 13
ST   DYS391: 10
ST   FGA: 20,24
ST   SE33: 19,23.2
ST   TH01: 6,9.3
ST   TPOX: 8,9
ST   vWA: 16,19
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   29Y
CA   Induced pluripotent stem cell
DT   Created: 15-11-17; Last updated: 19-12-24; Version: 8
//
RX   PubMed=28395737; DOI=10.1016/j.scr.2017.02.005;
RA   Narayanan G., Sheila M., Chai J., Stanton L.W.;
RT   "Generation of sibling-matched induced pluripotent stem cell lines
RT   from spinal and bulbar muscular atrophy patients.";
RL   Stem Cell Res. 20:30-33(2017).
//