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An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form on hereditary hemolytic anemia protein 4.2NIPPON

Author
BOUHASSIRA, E. E; SCHWARTZ, R. S; YAWATA, Y; ATA, K; KANZAKI, A; QIU, J. J.-H; NAGEL, R. L; RYBICKI, A. C
Albert Einstein coll. medicine, Montefiore medical cent., div. hematology, Bronx NY 10467, United States
Source

Blood. 1992, Vol 79, Num 7, pp 1846-1854 ; ref : 32 ref

ISSN
0006-4971
Scientific domain
Medical oncology; Hematology
Publisher
The Americain Society of Hematology, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Anémie hémolytique Biologie moléculaire Erythrocyte Homme Mongoloïde Race Protéine 4.2 Japon Hémopathie Maladie héréditaire Asie
Keyword (en)
Hemolytic anemia Molecular biology Red blood cell Human Mongoloid Race Japan Hemopathy Genetic disease Asia
Keyword (es)
Anemia hemolítica Biología molecular Eritrocito Hombre Mongoloide Raza Japón Hemopatía Enfermedad hereditaria Asia
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19A Diseases of red blood cells / 002B19A01 Anemias. Hemoglobinopathies

Discipline
Blood diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
5351526

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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