Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy. (Record no. 12243063)

MARC details
000 -LEADER
fixed length control field 01336 a2200385 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250514051957.0
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 1434-5161
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1007/s100380200091
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 Sudoyo, Herawati
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20030122
245 00 - TITLE STATEMENT
Title Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Journal of human genetics
Date of publication, distribution, etc. 2002
300 ## - PHYSICAL DESCRIPTION
Extent 594-604 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 Asia, Southeastern
General subdivision epidemiology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element DNA, Mitochondrial
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 Haplotypes
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 Mitochondria
General subdivision genetics
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 Optic Atrophy, Hereditary, Leber
General subdivision epidemiology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Phylogeny
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Polymorphism, Single Nucleotide
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Suryadi, Helena
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lertrit, Patcharee
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pramoonjago, Patcharin
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lyrawati, Diana
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Marzuki, Sangkot
773 0# - HOST ITEM ENTRY
Title Journal of human genetics
Related parts vol. 47
-- no. 11
-- p. 594-604
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1007/s100380200091">https://doi.org/10.1007/s100380200091</a>
Public note Available from publisher's website

No items available.