NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe. (Record no. 16771488)

MARC details
000 -LEADER
fixed length control field 01508 a2200493 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250515052759.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200801s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1364-6745
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1007/s10048-006-0074-9
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 Klebe, Stephan
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20080123
245 00 - TITLE STATEMENT
Title NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Neurogenetics
Date of publication, distribution, etc. Apr 2007
300 ## - PHYSICAL DESCRIPTION
Extent 155-7 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Letter; 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 Adult
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Age of Onset
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 Child
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Europe
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Exons
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 Genes, Dominant
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 Membrane Proteins
General subdivision genetics
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 Paraplegia
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lacour, Arnaud
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Durr, Alexandra
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Stojkovic, Tanya
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Depienne, Christel
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Forlani, Sylvie
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Poea-Guyon, Sandrine
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Vuillaume, Isabelle
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sablonniere, Bernard
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Vermersch, Patrick
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Brice, Alexis
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Stevanin, Giovanni
773 0# - HOST ITEM ENTRY
Title Neurogenetics
Related parts vol. 8
-- no. 2
-- p. 155-7
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1007/s10048-006-0074-9">https://doi.org/10.1007/s10048-006-0074-9</a>
Public note Available from publisher's website

No items available.