β-Spectrin StaBárbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism-Reference-Cited by-同舟云学术

β-Spectrin StaBárbara: a novel frameshift mutation in hereditary spherocytosis associated with detectable levels of mRNA and a germ cell line mosaicism

Published:2001-11 Issue:2 Volume:115 Page:347-353
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Bassères Daniela S.,Duarte Adriana S. S.,Hassoun Hani,Costa Fernando F.,Saad Sara T. O.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.03103.x/fullpdf

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3. Hereditary spherocytosis and related disorders;Becker;Clinical Haematology,1993

4. β-spectrin Kissimmee: a spectrin variant associated with autossomal dominant hereditary spherocytosis and defective binding to protein 4.1;Becker;Journal of Clinical Investigation,1993

5. Separation of leukocytes from blood and bone marrow;Boyum;Scandinavian Journal of Clinical and Laboratory Investigation. Supplement,1968

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