Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations. (Record no. 16727944)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 01382 a2200457 4500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250515051257.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 200701s 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.0000250254.67042.1b |
| 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 | Stogmann, E |
| 264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Date of production, publication, distribution, manufacture, or copyright notice | 20070108 |
| 245 00 - TITLE STATEMENT | |
| Title | Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations. |
| Medium | [electronic resource] |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Name of publisher, distributor, etc. | Neurology |
| Date of publication, distribution, etc. | Dec 2006 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 2029-31 p. |
| Other physical details | digital |
| 500 ## - GENERAL NOTE | |
| General note | Publication Type: Journal Article |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | 3' Untranslated Regions |
| General subdivision | genetics |
| 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 | Calcium-Binding Proteins |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Epilepsy, Generalized |
| General subdivision | genetics |
| 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 Variation |
| 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 | Mutation, Missense |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Phenotype |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Syndrome |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Lichtner, P |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Baumgartner, C |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Bonelli, S |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Assem-Hilger, E |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Leutmezer, F |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Schmied, M |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Hotzy, C |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Strom, T M |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Meitinger, T |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Zimprich, F |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Zimprich, A |
| 773 0# - HOST ITEM ENTRY | |
| Title | Neurology |
| Related parts | vol. 67 |
| -- | no. 11 |
| -- | p. 2029-31 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://doi.org/10.1212/01.wnl.0000250254.67042.1b">https://doi.org/10.1212/01.wnl.0000250254.67042.1b</a> |
| Public note | Available from publisher's website |
No items available.