000 01270 a2200397 4500
005 20250513095502.0
264 0 _c19961016
008 199610s 0 0 eng d
022 _a0364-5134
024 7 _a10.1002/ana.410400219
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aParano, E
245 0 0 _aMolecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy.
_h[electronic resource]
260 _bAnnals of neurology
_cAug 1996
300 _a247-51 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlleles
650 0 4 _aChild, Preschool
650 0 4 _aElectromyography
650 0 4 _aFamily
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aGenetic Variation
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aPhenotype
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Genetic
_xgenetics
650 0 4 _aSpinal Muscular Atrophies of Childhood
_xdiagnosis
700 1 _aPavone, L
700 1 _aFalsaperla, R
700 1 _aTrifiletti, R
700 1 _aWang, C
773 0 _tAnnals of neurology
_gvol. 40
_gno. 2
_gp. 247-51
856 4 0 _uhttps://doi.org/10.1002/ana.410400219
_zAvailable from publisher's website
999 _c8770381
_d8770381