Stepwise developmental regression associated with novel CACNA1A mutation. (Record no. 18403643)
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000 -LEADER | |
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fixed length control field | 01226 a2200361 4500 |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20250515143802.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
fixed length control field | 200812s 0 0 eng d |
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
International Standard Serial Number | 0887-8994 |
024 7# - OTHER STANDARD IDENTIFIER | |
Standard number or code | 10.1016/j.pediatrneurol.2008.07.030 |
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 | Guerin, Andrea A |
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
Date of production, publication, distribution, manufacture, or copyright notice | 20081219 |
245 00 - TITLE STATEMENT | |
Title | Stepwise developmental regression associated with novel CACNA1A mutation. |
Medium | [electronic resource] |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Name of publisher, distributor, etc. | Pediatric neurology |
Date of publication, distribution, etc. | Nov 2008 |
300 ## - PHYSICAL DESCRIPTION | |
Extent | 363-4 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 | Ataxia |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Calcium Channels |
General subdivision | genetics |
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 | Consciousness Disorders |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Epilepsy |
General subdivision | genetics |
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 | Humans |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Intellectual Disability |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Migraine with Aura |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Mutation, Missense |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Feigenbaum, Annette |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Donner, Elizabeth J |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Yoon, Grace |
773 0# - HOST ITEM ENTRY | |
Title | Pediatric neurology |
Related parts | vol. 39 |
-- | no. 5 |
-- | p. 363-4 |
856 40 - ELECTRONIC LOCATION AND ACCESS | |
Uniform Resource Identifier | <a href="https://doi.org/10.1016/j.pediatrneurol.2008.07.030">https://doi.org/10.1016/j.pediatrneurol.2008.07.030</a> |
Public note | Available from publisher's website |
No items available.