Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss. (Record no. 17544455)

MARC details
000 -LEADER
fixed length control field 01402 a2200385 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250515094618.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200802s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1399-0004
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1111/j.1399-0004.2007.00925.x
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 Labay, V
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20080229
245 00 - TITLE STATEMENT
Title Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Clinical genetics
Date of publication, distribution, etc. Jan 2008
300 ## - PHYSICAL DESCRIPTION
Extent 50-4 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element DNA, Mitochondrial
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Family Health
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genome, Mitochondrial
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Haplotypes
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hearing Loss, Sensorineural
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element North America
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 Point Mutation
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element RNA, Transfer, Ser
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Garrido, G
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Madeo, A C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Nance, W E
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Friedman, T B
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Friedman, P L
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Del Castillo, I
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Griffith, A J
773 0# - HOST ITEM ENTRY
Title Clinical genetics
Related parts vol. 73
-- no. 1
-- p. 50-4
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1111/j.1399-0004.2007.00925.x">https://doi.org/10.1111/j.1399-0004.2007.00925.x</a>
Public note Available from publisher's website

No items available.