000 01472 a2200397 4500
005 20250513035246.0
264 0 _c19950928
008 199509s 0 0 eng d
022 _a0885-3185
024 7 _a10.1002/mds.870100307
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPlanté-Bordeneuve, V
245 0 0 _aCYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.
_h[electronic resource]
260 _bMovement disorders : official journal of the Movement Disorder Society
_cMay 1995
300 _a277-8 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlleles
650 0 4 _aCytochrome P-450 CYP2D6
650 0 4 _aCytochrome P-450 Enzyme System
_xgenetics
650 0 4 _aDNA Mutational Analysis
650 0 4 _aGene Expression
_xphysiology
650 0 4 _aGene Frequency
_xgenetics
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aMixed Function Oxygenases
_xgenetics
650 0 4 _aOlivopontocerebellar Atrophies
_xgenetics
650 0 4 _aParkinson Disease
_xgenetics
650 0 4 _aPolymorphism, Genetic
_xgenetics
700 1 _aBandmann, O
700 1 _aWenning, G
700 1 _aQuinn, N P
700 1 _aDaniel, S E
700 1 _aHarding, A E
773 0 _tMovement disorders : official journal of the Movement Disorder Society
_gvol. 10
_gno. 3
_gp. 277-8
856 4 0 _uhttps://doi.org/10.1002/mds.870100307
_zAvailable from publisher's website
999 _c7650873
_d7650873