000 01183 a2200349 4500
005 20250513094919.0
264 0 _c19961126
008 199611s 0 0 eng d
022 _a0028-3878
024 7 _a10.1212/wnl.47.2.544
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aScoles, D R
245 0 0 _aA missense mutation in the neurofibromatosis 2 gene occurs in patients with mild and severe phenotypes.
_h[electronic resource]
260 _bNeurology
_cAug 1996
300 _a544-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aChromosome Mapping
650 0 4 _aGenes, Neurofibromatosis 2
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aNeurofibromatosis 2
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aPolymorphism, Single-Stranded Conformational
700 1 _aBaser, M E
700 1 _aPulst, S M
773 0 _tNeurology
_gvol. 47
_gno. 2
_gp. 544-6
856 4 0 _uhttps://doi.org/10.1212/wnl.47.2.544
_zAvailable from publisher's website
999 _c8753952
_d8753952