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Molecular characterization of two mutations in platelet glycoprotein (GP) Ibα in two Finnish Bernard-Soulier syndrome families

Author
KOSKELA, S1 ; PARTANEN, J1 ; SALMI, T. T2 ; KEKOMÄKI, R1
[1] Finnish Red Cross Blood Transfusion Service, 00310 Helsinki, Finland
[2] Turku University Central Hospital, 20500 Turku, Finland
Source

European journal of haematology. 1999, Vol 62, Num 3, pp 160-168 ; ref : 43 ref

CODEN
EJHAEC
ISSN
0902-4441
Scientific domain
Hematology
Publisher
Blackwell, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Dystrophie thrombocytaire Délétion Etude familiale Glycoprotéine Homme Mutation ponctuelle Protéine membranaire Thrombocyte Glycoprotéine Ibα Génétique Hémopathie Maladie héréditaire
Keyword (en)
Bernard Soulier disease Deletion Family study Glycoprotein Human Point mutation Membrane protein Platelet Genetics Hemopathy Genetic disease
Keyword (es)
Distrofia trombocitaria Deleción Estudio familiar Glicoproteína Hombre Mutación puntual Proteína membranar Trombocito Genética Hemopatía Enfermedad hereditaria
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19C Platelet diseases and coagulopathies

Discipline
Blood diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
1765485

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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