The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome. (Record no. 17810507)

MARC details
000 -LEADER
fixed length control field 01540 a2200433 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250515111643.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200808s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1531-8257
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/mds.21970
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 Rossi, Giacomina
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20080806
245 00 - TITLE STATEMENT
Title The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.
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. Apr 2008
300 ## - PHYSICAL DESCRIPTION
Extent 892-5 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Adult
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Amino Acid Substitution
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Basal Ganglia
General subdivision pathology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Brain Diseases
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Cerebral Cortex
General subdivision pathology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosomes, Human, Pair 17
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Dementia
General subdivision genetics
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 Parkinson Disease
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Tauopathies
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Tremor
General subdivision etiology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element tau Proteins
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Marelli, Cecilia
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Farina, Laura
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Laurà, Matilde
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Maria Basile, Anna
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ciano, Claudia
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tagliavini, Fabrizio
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pareyson, Davide
773 0# - HOST ITEM ENTRY
Title Movement disorders : official journal of the Movement Disorder Society
Related parts vol. 23
-- no. 6
-- p. 892-5
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/mds.21970">https://doi.org/10.1002/mds.21970</a>
Public note Available from publisher's website

No items available.