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Two point mutations are responsible for G6PD polymorphism in Sardinia

Author
DE VITA, G1 ; ALCALAY, M; SAMPIETRO, M; DOMENICA CAPPELINI, M; FIORELLI, G; TONIOLO, D
[1] CNR, ist. internazionale genetica biofisica, Naples, Italy
Source

American journal of human genetics. 1989, Vol 44, Num 2, pp 233-240 ; ref : 2 p

CODEN
AJHGAG
ISSN
0002-9297
Scientific domain
Genetics
Publisher
University of Chicago Press, Chicago, IL
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Carte génétique Déficit Enzyme Enzymopathie Etude familiale Glucose-6-phosphate dehydrogenase Génétique population Homme Hémopathie Linkage Maladie héréditaire Mutation ponctuelle Polymorphisme Sardaigne Séquence nucléotide Variant génétique Europe Italie
Keyword (en)
Genetic mapping Deficiency Enzyme Enzymopathy Family study Glucose-6-phosphate dehydrogenase Population genetics Human Hemopathy Linkage Genetic disease Point mutation Polymorphism Sardinia Nucleotide sequence Genetic variant Europe Italy
Keyword (es)
Mapa genético Déficiencia Enzima Enzimopatía Estudio familiar Glucose-6-phosphate dehydrogenase Genética población Hombre Hemopatía Ligamiento Enfermedad hereditaria Mutación puntual Polimorfismo Cerdeña Secuencia nucleótido Variante genética Europa Italia
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
7141080

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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