Pyruvate carboxylase deficiencies: complementation studies between "French" and "American" phenotypes in cultured fibroblasts. (Record no. 3945217)

MARC details
000 -LEADER
fixed length control field 01345 a2200373 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250512081220.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 198701s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0141-8955
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1007/BF01801665
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 Augereau, C
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19870109
245 00 - TITLE STATEMENT
Title Pyruvate carboxylase deficiencies: complementation studies between "French" and "American" phenotypes in cultured fibroblasts.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Journal of inherited metabolic disease
Date of publication, distribution, etc. 1985
300 ## - PHYSICAL DESCRIPTION
Extent 59-62 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Comparative Study; Journal Article
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Amino Acid Metabolism, Inborn Errors
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Cells, Cultured
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Fibroblasts
General subdivision enzymology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genetic Complementation Test
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 Multiple Carboxylase Deficiency
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 Phenotype
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pyruvate Carboxylase
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pyruvate Carboxylase Deficiency Disease
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pham Dinh, D
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Moncion, A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Marsac, C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Saudubray, J M
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Robinson, B H
773 0# - HOST ITEM ENTRY
Title Journal of inherited metabolic disease
Related parts vol. 8
-- no. 2
-- p. 59-62
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1007/BF01801665">https://doi.org/10.1007/BF01801665</a>
Public note Available from publisher's website

No items available.