hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. (Record no. 23165318)
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000 -LEADER | |
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fixed length control field | 01625 a2200433 4500 |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20250516173938.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
fixed length control field | 201409s 0 0 eng d |
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
International Standard Serial Number | 1558-1497 |
024 7# - OTHER STANDARD IDENTIFIER | |
Standard number or code | 10.1016/j.neurobiolaging.2013.09.016 |
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 | Le Ber, Isabelle |
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
Date of production, publication, distribution, manufacture, or copyright notice | 20140929 |
245 00 - TITLE STATEMENT | |
Title | hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. |
Medium | [electronic resource] |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Name of publisher, distributor, etc. | Neurobiology of aging |
Date of publication, distribution, etc. | Apr 2014 |
300 ## - PHYSICAL DESCRIPTION | |
Extent | 934.e5-6 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 | Amyotrophic Lateral Sclerosis |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Cohort Studies |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Frontotemporal Lobar Degeneration |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Heterogeneous Nuclear Ribonucleoprotein A1 |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Heterogeneous-Nuclear Ribonucleoprotein Group A-B |
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 | Myositis, Inclusion Body |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Osteitis Deformans |
General subdivision | genetics |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Van Bortel, Inge |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Nicolas, Gael |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Bouya-Ahmed, Kawtar |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Camuzat, Agnès |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Wallon, David |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | De Septenville, Anne |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Latouche, Morwena |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Lattante, Serena |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Kabashi, Edor |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Jornea, Ludmila |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Hannequin, Didier |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Brice, Alexis |
773 0# - HOST ITEM ENTRY | |
Title | Neurobiology of aging |
Related parts | vol. 35 |
-- | no. 4 |
-- | p. 934.e5-6 |
856 40 - ELECTRONIC LOCATION AND ACCESS | |
Uniform Resource Identifier | <a href="https://doi.org/10.1016/j.neurobiolaging.2013.09.016">https://doi.org/10.1016/j.neurobiolaging.2013.09.016</a> |
Public note | Available from publisher's website |
No items available.