000 01102 a2200313 4500
005 20250511183406.0
264 0 _c19921113
008 199211s 0 0 eng d
022 _a0364-5134
024 7 _a10.1002/ana.410320318
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBoylan, K B
245 0 0 _aWerdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
_h[electronic resource]
260 _bAnnals of neurology
_cSep 1992
300 _a404-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMuscular Atrophy, Spinal
_xcomplications
650 0 4 _aPedigree
650 0 4 _aSpinal Muscular Atrophies of Childhood
_xcomplications
700 1 _aCornblath, D R
773 0 _tAnnals of neurology
_gvol. 32
_gno. 3
_gp. 404-7
856 4 0 _uhttps://doi.org/10.1002/ana.410320318
_zAvailable from publisher's website
999 _c1423303
_d1423303