Gene symbol: MECP2. Disease: Rett syndrome. (Record no. 16699353)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 01042 a2200361 4500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250515050318.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 200612s 0 0 eng d |
| 022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
| International Standard Serial Number | 0340-6717 |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | NLM |
| Language of cataloging | eng |
| Transcribing agency | NLM |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Conforti, F L |
| 264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Date of production, publication, distribution, manufacture, or copyright notice | 20061207 |
| 245 00 - TITLE STATEMENT | |
| Title | Gene symbol: MECP2. Disease: Rett syndrome. |
| Medium | [electronic resource] |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Name of publisher, distributor, etc. | Human genetics |
| Date of publication, distribution, etc. | Jul 2006 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 676 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 | Amino Acid Substitution |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Asparagine |
| General subdivision | genetics |
| 650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
| Topical term or geographic name entry element | Codon, Nonsense |
| 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 | Methyl-CpG-Binding Protein 2 |
| General subdivision | genetics |
| 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 | Rett Syndrome |
| General subdivision | genetics |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Mazzei, R |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Sprovieri, T |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Ungaro, C |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Patitucci, A |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Magariello, A |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Gabriele, A L |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Bravaccio, C |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Muglia, M |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Quattrone, A |
| 773 0# - HOST ITEM ENTRY | |
| Title | Human genetics |
| Related parts | vol. 119 |
| -- | no. 6 |
| -- | p. 676 |
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