000 01682 a2200529 4500
005 20250515040325.0
264 0 _c20061128
008 200611s 0 0 eng d
022 _a0960-8966
024 7 _a10.1016/j.nmd.2006.06.008
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKlinge, Lars
245 0 0 _aSevere phenotype in infantile facioscapulohumeral muscular dystrophy.
_h[electronic resource]
260 _bNeuromuscular disorders : NMD
_cOct 2006
300 _a553-8 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aCohort Studies
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDisease Progression
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aGenetic Testing
650 0 4 _aHumans
650 0 4 _aInheritance Patterns
_xgenetics
650 0 4 _aLongitudinal Studies
650 0 4 _aLordosis
_xgenetics
650 0 4 _aMale
650 0 4 _aMosaicism
650 0 4 _aMuscle Weakness
_xgenetics
650 0 4 _aMuscle, Skeletal
_xmetabolism
650 0 4 _aMuscular Atrophy
_xgenetics
650 0 4 _aMuscular Dystrophy, Facioscapulohumeral
_xdiagnosis
650 0 4 _aMutation
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aPrognosis
650 0 4 _aSex Distribution
700 1 _aEagle, Michelle
700 1 _aHaggerty, Irene D
700 1 _aRoberts, Catherine E
700 1 _aStraub, Volker
700 1 _aBushby, Kate M
773 0 _tNeuromuscular disorders : NMD
_gvol. 16
_gno. 9-10
_gp. 553-8
856 4 0 _uhttps://doi.org/10.1016/j.nmd.2006.06.008
_zAvailable from publisher's website
999 _c16520273
_d16520273