Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene. (Record no. 15412550)

MARC details
000 -LEADER
fixed length control field 01594 a2200445 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250514220930.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200505s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0027-8424
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1073/pnas.0500517102
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 Tanner, Stephan M
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20050509
245 00 - TITLE STATEMENT
Title Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Proceedings of the National Academy of Sciences of the United States of America
Date of publication, distribution, etc. Mar 2005
300 ## - PHYSICAL DESCRIPTION
Extent 4130-3 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosome Mapping
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosomes, Human, Pair 11
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 Intrinsic Factor
General subdivision genetics
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 Pedigree
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Vitamin B 12
General subdivision metabolism
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Vitamin B 12 Deficiency
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Li, Zhongyuan
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Perko, James D
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Oner, Cihan
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Cetin, Mualla
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Altay, Cigdem
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Yurtsever, Zekiye
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name David, Karen L
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Faivre, Laurence
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ismail, Essam A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Gräsbeck, Ralph
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name de la Chapelle, Albert
773 0# - HOST ITEM ENTRY
Title Proceedings of the National Academy of Sciences of the United States of America
Related parts vol. 102
-- no. 11
-- p. 4130-3
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1073/pnas.0500517102">https://doi.org/10.1073/pnas.0500517102</a>
Public note Available from publisher's website

No items available.