ID   HPS1358
AC   CVCL_YQ69
DR   RCB; HPS1358
DR   Wikidata; Q94219690
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex49-52del; Zygosity=Hemizygous (RCB=HPS1358).
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_UN73 ! HPS1355
OI   CVCL_YQ67 ! HPS1356
OI   CVCL_YQ68 ! HPS1357
OI   CVCL_YQ70 ! HPS1359
OI   CVCL_YQ71 ! HPS1360
SX   Male
AG   40-49Y
CA   Induced pluripotent stem cell
DT   Created: 12-03-20; Last updated: 19-12-24; Version: 6
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