000 01310 a2200349 4500
005 20250517151630.0
264 0 _c20180418
008 201804s 0 0 eng d
022 _a1872-7131
024 7 _a10.1016/j.braindev.2017.04.007
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTavasoli, Ali Reza
245 0 0 _aEarly infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: A case report and literature review.
_h[electronic resource]
260 _bBrain & development
_cSep 2017
300 _a714-716 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Review
650 0 4 _aBrain
_xdiagnostic imaging
650 0 4 _aChild, Preschool
650 0 4 _aDevelopmental Disabilities
_xdiagnostic imaging
650 0 4 _aEnoyl-CoA Hydratase
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMetabolism, Inborn Errors
_xdiagnostic imaging
650 0 4 _aMutation
650 0 4 _aRNA-Binding Proteins
_xgenetics
700 1 _aShervin Badv, Reza
700 1 _aZschocke, Johannes
700 1 _aAshrafi, Mahmood Reza
700 1 _aRostami, Parastoo
773 0 _tBrain & development
_gvol. 39
_gno. 8
_gp. 714-716
856 4 0 _uhttps://doi.org/10.1016/j.braindev.2017.04.007
_zAvailable from publisher's website
999 _c27109050
_d27109050