Inherited myoclonus-dystonia: evidence supporting genetic heterogeneity. (Record no. 11153455)

MARC details
000 -LEADER
fixed length control field 01469 a2200397 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250513232228.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200106s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0885-3185
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/1531-8257(200101)16:1<106::aid-mds1022>3.0.co;2-7
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 Grimes, D A
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20010614
245 00 - TITLE STATEMENT
Title Inherited myoclonus-dystonia: evidence supporting genetic heterogeneity.
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. Jan 2001
300 ## - PHYSICAL DESCRIPTION
Extent 106-10 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 Adolescent
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Child
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Child, Preschool
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosomes, Human, Pair 11
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Dystonic Disorders
General subdivision complications
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Female
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genetic Linkage
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 Male
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Myoclonus
General subdivision complications
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pedigree
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Point Mutation
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Polymerase Chain Reaction
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Receptors, Dopamine D2
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bulman, D
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name George-Hyslop, P S
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lang, A E
773 0# - HOST ITEM ENTRY
Title Movement disorders : official journal of the Movement Disorder Society
Related parts vol. 16
-- no. 1
-- p. 106-10
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/1531-8257(200101)16:1<106::aid-mds1022>3.0.co;2-7">https://doi.org/10.1002/1531-8257(200101)16:1<106::aid-mds1022>3.0.co;2-7</a>
Public note Available from publisher's website

No items available.