Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas). (Record no. 8701458)

MARC details
000 -LEADER
fixed length control field 01291 a2200385 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250513093144.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 199609s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0006-4971
040 ## - CATALOGING SOURCE
Original cataloging agency NLM
Language of cataloging eng
Transcribing agency NLM
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Alloisio, N
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19960912
245 00 - TITLE STATEMENT
Title Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas).
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Blood
Date of publication, distribution, etc. Aug 1996
300 ## - PHYSICAL DESCRIPTION
Extent 1062-9 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Alleles
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Anion Exchange Protein 1, Erythrocyte
General subdivision deficiency
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Base Sequence
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Heterozygote
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 Infant
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 Molecular Sequence Data
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 Polymorphism, Single-Stranded Conformational
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Spherocytosis, Hereditary
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Maillet, P
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Carré, G
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Texier, P
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Vallier, A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Baklouti, F
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Philippe, N
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Delaunay, J
773 0# - HOST ITEM ENTRY
Title Blood
Related parts vol. 88
-- no. 3
-- p. 1062-9

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