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Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis.
Alloisio, N; Texier, P; Vallier, A; Ribeiro, M L; Morlé, L; Bozon, M; Bursaux, E; Maillet, P; Gonçalves, P; Tanner, M J; Tamagnini, G; Delaunay, J.
Affiliation
  • Alloisio N; Laboratoire de Génétique Moléculaire Humaine, Centre National de la Recherche Scientifique, URA 1171, Institut Pasteur de Lyon, France.
Blood ; 90(1): 414-20, 1997 Jul 01.
Article in En | MEDLINE | ID: mdl-9207478
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Collection: 01-internacional Database: MEDLINE Main subject: Spherocytosis, Hereditary / Anion Exchange Protein 1, Erythrocyte / Alleles Limits: Female / Humans / Male Language: En Journal: Blood Year: 1997 Document type: Article Affiliation country: Francia Country of publication: Estados Unidos
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Spherocytosis, Hereditary / Anion Exchange Protein 1, Erythrocyte / Alleles Limits: Female / Humans / Male Language: En Journal: Blood Year: 1997 Document type: Article Affiliation country: Francia Country of publication: Estados Unidos