000 01194 a2200361 4500
005 20250518010701.0
264 0 _c20191230
008 201912s 0 0 eng d
022 _a1439-1899
024 7 _a10.1055/s-0038-1675626
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aArdıçlı, Didem
245 0 0 _aDiagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience.
_h[electronic resource]
260 _bNeuropediatrics
_c02 2019
300 _a41-45 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aCodon, Nonsense
_xgenetics
650 0 4 _aDystrophin
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMuscular Dystrophy, Duchenne
_xdiagnosis
650 0 4 _aMutation
_xgenetics
650 0 4 _aRetrospective Studies
650 0 4 _aTertiary Care Centers
700 1 _aHaliloğlu, Goknur
700 1 _aAlikaşifoğlu, Mehmet
700 1 _aTopaloğlu, Haluk
773 0 _tNeuropediatrics
_gvol. 50
_gno. 1
_gp. 41-45
856 4 0 _uhttps://doi.org/10.1055/s-0038-1675626
_zAvailable from publisher's website
999 _c29068468
_d29068468