CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy. (Record no. 7650873)

MARC details
000 -LEADER
fixed length control field 01472 a2200397 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250513035246.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 199509s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0885-3185
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/mds.870100307
Source of number or code doi
040 ## - CATALOGING SOURCE
Original cataloging agency NLM
Language of cataloging eng
Transcribing agency NLM
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Planté-Bordeneuve, V
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19950928
245 00 - TITLE STATEMENT
Title CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Movement disorders : official journal of the Movement Disorder Society
Date of publication, distribution, etc. May 1995
300 ## - PHYSICAL DESCRIPTION
Extent 277-8 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, Non-U.S. Gov't
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Alleles
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Cytochrome P-450 CYP2D6
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Cytochrome P-450 Enzyme System
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element DNA Mutational Analysis
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Gene Expression
General subdivision physiology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Gene Frequency
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genotype
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Humans
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mixed Function Oxygenases
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Olivopontocerebellar Atrophies
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Parkinson Disease
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Polymorphism, Genetic
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bandmann, O
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Wenning, G
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Quinn, N P
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Daniel, S E
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Harding, A E
773 0# - HOST ITEM ENTRY
Title Movement disorders : official journal of the Movement Disorder Society
Related parts vol. 10
-- no. 3
-- p. 277-8
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/mds.870100307">https://doi.org/10.1002/mds.870100307</a>
Public note Available from publisher's website

No items available.