000 01499 a2200481 4500
005 20250517162833.0
264 0 _c20190730
008 201907s 0 0 eng d
022 _a1399-0004
024 7 _a10.1111/cge.13093
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSkakic, A
245 0 0 _aGenetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants.
_h[electronic resource]
260 _bClinical genetics
_c02 2018
300 _a350-355 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlleles
650 0 4 _aAntiporters
_xgenetics
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aFemale
650 0 4 _aGenetics, Population
650 0 4 _aGenotype
650 0 4 _aGlycogen Storage Disease Type I
_xgenetics
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMonosaccharide Transport Proteins
_xgenetics
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aSerbia
_xepidemiology
700 1 _aDjordjevic, M
700 1 _aSarajlija, A
700 1 _aKlaassen, K
700 1 _aTosic, N
700 1 _aKecman, B
700 1 _aUgrin, M
700 1 _aSpasovski, V
700 1 _aPavlovic, S
700 1 _aStojiljkovic, M
773 0 _tClinical genetics
_gvol. 93
_gno. 2
_gp. 350-355
856 4 0 _uhttps://doi.org/10.1111/cge.13093
_zAvailable from publisher's website
999 _c27346447
_d27346447