A new NBIA patient from Turkey with homozygous C19ORF12 mutation. (Record no. 28916853)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 01224 a2200373 4500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250518002248.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 202004s 0 0 eng d |
| 022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
| International Standard Serial Number | 2240-2993 |
| 024 7# - OTHER STANDARD IDENTIFIER | |
| Standard number or code | 10.1007/s13760-018-1026-5 |
| 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 | Kasapkara, Çiğdem Seher |
| 264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Date of production, publication, distribution, manufacture, or copyright notice | 20200406 |
| 245 00 - TITLE STATEMENT | |
| Title | A new NBIA patient from Turkey with homozygous C19ORF12 mutation. |
| Medium | [electronic resource] |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Name of publisher, distributor, etc. | Acta neurologica Belgica |
| Date of publication, distribution, etc. | Dec 2019 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 623-625 p. |
| Other physical details | digital |
| 500 ## - GENERAL NOTE | |
| General note | Publication Type: Case Reports; Letter |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Homozygote |
| 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 | Iron Metabolism Disorders |
| General subdivision | genetics |
| 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 | Mutation |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Neuroaxonal Dystrophies |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Turkey |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Tümer, Leyla |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Gregory, Allison |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Ezgü, Fatih |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | İnci, Aslı |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Derinkuyu, Betül Emine |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Fox, Rachel |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Rogers, Caleb |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Hayflick, Susan |
| 773 0# - HOST ITEM ENTRY | |
| Title | Acta neurologica Belgica |
| Related parts | vol. 119 |
| -- | no. 4 |
| -- | p. 623-625 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://doi.org/10.1007/s13760-018-1026-5">https://doi.org/10.1007/s13760-018-1026-5</a> |
| Public note | Available from publisher's website |
No items available.