Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.

Hassoun, H; Vassiliadis, J N; Murray, J; Njolstad, P R; Rogus, J J; Ballas, S K; Schaffer, F; Jarolim, P; Brabec, V; Palek, J

Hassoun, H; Vassiliadis, J N; Murray, J; Njolstad, P R; Rogus, J J; Ballas, S K; Schaffer, F; Jarolim, P; Brabec, V; Palek, J.

Affiliation

Hassoun H; Department of Biomedical Research, St Elizabeth's Medical Center of Boston, Tufts University Medical School, MA 02135, USA.

Blood ; 90(1): 398-406, 1997 Jul 01.

Article in En | MEDLINE | ID: mdl-9207476

Subject(s)

Spectrin/genetics; Spherocytosis, Hereditary/genetics; DNA, Complementary/genetics; Female; Frameshift Mutation; Humans; Male; Pedigree; Spectrin/deficiency; Spherocytosis, Hereditary/metabolism

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Collection: 01-internacional Database: MEDLINE Main subject: Spherocytosis, Hereditary / Spectrin Type of study: Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Blood Year: 1997 Document type: Article

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