NTNG1 mutations are a rare cause of Rett syndrome. (Record no. 16113102)

MARC details
000 -LEADER
fixed length control field 01598 a2200493 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250515015539.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200605s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1552-4825
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/ajmg.a.31133
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 Archer, Hayley L
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20060530
245 00 - TITLE STATEMENT
Title NTNG1 mutations are a rare cause of Rett syndrome.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. American journal of medical genetics. Part A
Date of publication, distribution, etc. Apr 2006
300 ## - PHYSICAL DESCRIPTION
Extent 691-4 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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 Female
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element GPI-Linked Proteins
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Gene Frequency
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Glycoproteins
General subdivision genetics
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
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Nerve Tissue Proteins
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Netrins
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 Evans, Julie C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Millar, David S
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Thompson, Peter W
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kerr, Alison M
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Leonard, Helen
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Christodoulou, John
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ravine, David
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lazarou, Lazarus
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Grove, Lucy
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Verity, Christopher
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Whatley, Sharon D
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pilz, Daniela T
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sampson, Julian R
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Clarke, Angus J
773 0# - HOST ITEM ENTRY
Title American journal of medical genetics. Part A
Related parts vol. 140
-- no. 7
-- p. 691-4
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/ajmg.a.31133">https://doi.org/10.1002/ajmg.a.31133</a>
Public note Available from publisher's website

No items available.