000 01323 a2200409 4500
005 20250517044528.0
264 0 _c20160621
008 201606s 0 0 eng d
022 _a1362-4962
024 7 _a10.1093/nar/gkv772
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMignardi, Marco
245 0 0 _aOligonucleotide gap-fill ligation for mutation detection and sequencing in situ.
_h[electronic resource]
260 _bNucleic acids research
_cDec 2015
300 _ae151 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aCell Line
650 0 4 _aCell Line, Tumor
650 0 4 _aCells, Cultured
650 0 4 _aDNA Mutational Analysis
_xmethods
650 0 4 _aDNA, Mitochondrial
_xchemistry
650 0 4 _aDNA, Neoplasm
_xchemistry
650 0 4 _aHumans
650 0 4 _aMice
650 0 4 _aOligonucleotides
650 0 4 _aPoint Mutation
650 0 4 _aRNA, Messenger
_xchemistry
700 1 _aMezger, Anja
700 1 _aQian, Xiaoyan
700 1 _aLa Fleur, Linnea
700 1 _aBotling, Johan
700 1 _aLarsson, Chatarina
700 1 _aNilsson, Mats
773 0 _tNucleic acids research
_gvol. 43
_gno. 22
_gp. e151
856 4 0 _uhttps://doi.org/10.1093/nar/gkv772
_zAvailable from publisher's website
999 _c25137376
_d25137376