De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy. (Record no. 23215618)

MARC details
000 -LEADER
fixed length control field 01534 a2200469 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250516175730.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201401s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1526-632X
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1212/01.wnl.0000436615.58705.c9
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 Mademan, Inès
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20140121
245 00 - TITLE STATEMENT
Title De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Neurology
Date of publication, distribution, etc. Nov 2013
300 ## - PHYSICAL DESCRIPTION
Extent 1953-8 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 Adult
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Charcot-Marie-Tooth Disease
General subdivision complications
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element DNA Mutational Analysis
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Family Health
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 Formins
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Glomerulosclerosis, Focal Segmental
General subdivision complications
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 Microfilament Proteins
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Models, Molecular
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Young Adult
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Deconinck, Tine
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Dinopoulos, Argirios
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Voit, Thomas
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Schara, Ulrike
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Devriendt, Koenraad
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Meijers, Björn
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lerut, Evelyne
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name De Jonghe, Peter
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Baets, Jonathan
773 0# - HOST ITEM ENTRY
Title Neurology
Related parts vol. 81
-- no. 22
-- p. 1953-8
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1212/01.wnl.0000436615.58705.c9">https://doi.org/10.1212/01.wnl.0000436615.58705.c9</a>
Public note Available from publisher's website

No items available.