000 01204 a2200349 4500
005 20250517181342.0
264 0 _c20180703
008 201807s 0 0 eng d
022 _a1876-7753
024 7 _a10.1016/j.scr.2017.08.017
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aZurita-Díaz, Francisco
245 0 0 _aEstablishment of a human DOA 'plus' iPSC line, IISHDOi003-A, with the mutation in the OPA1 gene: c.1635C>A; p.Ser545Arg.
_h[electronic resource]
260 _bStem cell research
_c10 2017
300 _a81-84 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aCell Line
650 0 4 _aGTP Phosphohydrolases
_xgenetics
650 0 4 _aHumans
650 0 4 _aKruppel-Like Factor 4
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aOptic Atrophy, Autosomal Dominant
_xgenetics
700 1 _aGalera-Monge, Teresa
700 1 _aMoreno-Izquierdo, Ana
700 1 _aCorton, Marta
700 1 _aAyuso, Carmen
700 1 _aGaresse, Rafael
700 1 _aGallardo, M Esther
773 0 _tStem cell research
_gvol. 24
_gp. 81-84
856 4 0 _uhttps://doi.org/10.1016/j.scr.2017.08.017
_zAvailable from publisher's website
999 _c27687630
_d27687630