Prenatal human ocular degeneration occurs in Leber's congenital amaurosis (LCA2). (Record no. 12015472)

MARC details
000 -LEADER
fixed length control field 01360 a2200409 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250514040406.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200301s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1099-498X
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/jgm.278
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 Porto, Fernanda B O
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20030116
245 00 - TITLE STATEMENT
Title Prenatal human ocular degeneration occurs in Leber's congenital amaurosis (LCA2).
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. The journal of gene medicine
Date of publication, distribution, etc.
300 ## - PHYSICAL DESCRIPTION
Extent 390-6 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, Non-U.S. Gov't
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Aborted Fetus
General subdivision pathology
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 Immunohistochemistry
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Lod Score
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 Optic Atrophy, Hereditary, Leber
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pedigree
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Retina
General subdivision pathology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Retinal Cone Photoreceptor Cells
General subdivision immunology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Rod Opsins
General subdivision immunology
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Perrault, Isabelle
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Hicks, David
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Rozet, Jean-Michel
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Hanoteau, Noëlle
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Hanein, Sylvain
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kaplan, Josseline
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sahel, José Alain
773 0# - HOST ITEM ENTRY
Title The journal of gene medicine
Related parts vol. 4
-- no. 4
-- p. 390-6
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/jgm.278">https://doi.org/10.1002/jgm.278</a>
Public note Available from publisher's website

No items available.