000 01527 a2200481 4500
005 20250515095515.0
264 0 _c20080219
008 200802s 0 0 eng d
022 _a0887-8994
024 7 _a10.1016/j.pediatrneurol.2007.09.006
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCeulemans, Berten P
245 0 0 _aMuscle pain as the only presenting symptom in a girl with dystrophinopathy.
_h[electronic resource]
260 _bPediatric neurology
_cJan 2008
300 _a64-6 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAge of Onset
650 0 4 _aChild, Preschool
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDisease Progression
650 0 4 _aDystrophin
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aGenetic Markers
_xgenetics
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aInheritance Patterns
_xgenetics
650 0 4 _aMale
650 0 4 _aMuscle, Skeletal
_xmetabolism
650 0 4 _aMuscular Dystrophy, Duchenne
_xdiagnosis
650 0 4 _aMutation
_xgenetics
650 0 4 _aPain
_xgenetics
650 0 4 _aPedigree
650 0 4 _aSex Factors
700 1 _aStorm, Katrien
700 1 _aReyniers, Edwin
700 1 _aCallewaert, Luc
700 1 _aMartin, Jean Jacques
773 0 _tPediatric neurology
_gvol. 38
_gno. 1
_gp. 64-6
856 4 0 _uhttps://doi.org/10.1016/j.pediatrneurol.2007.09.006
_zAvailable from publisher's website
999 _c17569110
_d17569110