Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease-Reference-Cited by-同舟云学术

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Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease

Published:1996-09 Issue:3 Volume:10 Page:129-147
ISSN:0268-960X
Container-title:Blood Reviews
language:en
Short-container-title:Blood Reviews

Author:

Hassoun H.,Palek J.

Publisher

Elsevier BV

Subject

Oncology,Hematology

Reference128 articles.

1. The spectrin-based membrane skeleton and micron-scale organization of the plasma membrane;Bennett;Annu Rev Cell Biol,1993

2. Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins;Palek;Blood Rev,1987

3. Mutations of the red blood cell membrane proteins: from clinical evaluations to detection of the underlying genetic defect;Palek;Blood,1992

4. The molecular structure of human erythrocyte spectrin. Biophysical and electron microscopic studies;Shotton;J Mol Biol,1979

5. Oligomeric states of spectrin in normal erythrocyte membranes: biochemical and electron microscopic studies;Liu;Cell,1984

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