ID   HPS1369
AC   CVCL_A3TE
DR   RCB; HPS1369
DR   Wikidata; Q105507924
CC   Sequence variation: Mutation; HGNC; 2928; DMD; Unexplicit; Ex3-7del; Zygosity=Hemizygous (RCB=HPS1369).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_UN74 ! HPS1367
OI   CVCL_A3TD ! HPS1368
OI   CVCL_A3TF ! HPS1370
OI   CVCL_A3TG ! HPS1371
OI   CVCL_A3TH ! HPS1372
SX   Male
AG   30-39Y
CA   Induced pluripotent stem cell
DT   Created: 12-01-21; Last updated: 29-06-23; Version: 4
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