Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy. (Record no. 25787556)
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fixed length control field | 01440 a2200421 4500 |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20250517083028.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
fixed length control field | 201711s 0 0 eng d |
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
International Standard Serial Number | 1744-5094 |
024 7# - OTHER STANDARD IDENTIFIER | |
Standard number or code | 10.3109/13816810.2015.1120316 |
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 | Kondo, Hiroyuki |
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
Date of production, publication, distribution, manufacture, or copyright notice | 20171117 |
245 00 - TITLE STATEMENT | |
Title | Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy. |
Medium | [electronic resource] |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Name of publisher, distributor, etc. | Ophthalmic genetics |
Date of publication, distribution, etc. | 12 2016 |
300 ## - PHYSICAL DESCRIPTION | |
Extent | 462-464 p. |
Other physical details | digital |
500 ## - GENERAL NOTE | |
General note | Publication Type: Letter; Research Support, Non-U.S. Gov't |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Base Sequence |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Basic Helix-Loop-Helix Transcription Factors |
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 | DNA Mutational Analysis |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Eye Diseases, Hereditary |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Familial Exudative Vitreoretinopathies |
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 | 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 | Infant |
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 | Molecular Sequence Data |
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 | Retinal Diseases |
General subdivision | congenital |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Sequence Deletion |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Matsushita, Itsuka |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Tahira, Tomoko |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Uchio, Eiichi |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Kusaka, Shunji |
773 0# - HOST ITEM ENTRY | |
Title | Ophthalmic genetics |
Related parts | vol. 37 |
-- | no. 4 |
-- | p. 462-464 |
856 40 - ELECTRONIC LOCATION AND ACCESS | |
Uniform Resource Identifier | <a href="https://doi.org/10.3109/13816810.2015.1120316">https://doi.org/10.3109/13816810.2015.1120316</a> |
Public note | Available from publisher's website |
No items available.