A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease. (Record no. 7902305)

MARC details
000 -LEADER
fixed length control field 01382 a2200445 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250513051145.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 199401s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0028-3878
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1212/wnl.43.12.2723-a
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 Yamada, M
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19940113
245 00 - TITLE STATEMENT
Title A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Neurology
Date of publication, distribution, etc. Dec 1993
300 ## - PHYSICAL DESCRIPTION
Extent 2723-4 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Journal Article
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Base Sequence
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Codon
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genes
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Gerstmann-Straussler-Scheinker Disease
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 Middle Aged
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Molecular Sequence Data
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Polymorphism, Genetic
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PrPSc Proteins
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Prions
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Itoh, Y
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Fujigasaki, H
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Naruse, S
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kaneko, K
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kitamoto, T
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tateishi, J
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Otomo, E
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Hayakawa, M
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tanaka, J
773 0# - HOST ITEM ENTRY
Title Neurology
Related parts vol. 43
-- no. 12
-- p. 2723-4
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1212/wnl.43.12.2723-a">https://doi.org/10.1212/wnl.43.12.2723-a</a>
Public note Available from publisher's website

No items available.