CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy. (Record no. 25001921)

MARC details
000 -LEADER
fixed length control field 01390 a2200409 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250517035955.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201601s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1531-8249
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/ana.24464
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 Morel, Godelieve
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20160126
245 00 - TITLE STATEMENT
Title CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Annals of neurology
Date of publication, distribution, etc. Nov 2015
300 ## - PHYSICAL DESCRIPTION
Extent 831 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Letter; Research Support, Non-U.S. Gov't; Comment
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 Predisposition to 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 Mitochondrial Proteins
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Muscular Atrophy, Spinal
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Rouzier, Cécile
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Chaussenot, Annabelle
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ait-El-Mkadem, Samira
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bannwarth, Sylvie
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Genin, Emmanuelle C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Augé, Gaëlle
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Chabrol, Brigitte
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pouget, Jean
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Soriani, Marie Hélène
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sacconi, Sabrina
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Paquis-Flucklinger, Véronique
773 0# - HOST ITEM ENTRY
Title Annals of neurology
Related parts vol. 78
-- no. 5
-- p. 831
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/ana.24464">https://doi.org/10.1002/ana.24464</a>
Public note Available from publisher's website

No items available.