Hematologically important mutations: spectrin and ...[Blood Cells Mol Dis. 1998]

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1: Blood Cells Mol Dis. 1998 Dec;24(4):539-43. Links

Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.

Department of Pediatrics, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06520-8064, USA.

PMID: 9887280 [PubMed - indexed for MEDLINE]

Hematologically important mutations: ankyrin variants in hereditary spherocytosis.
Blood Cells Mol Dis. 2005 Nov-Dec; 35(3):345-7. Epub 2005 Oct 11.

[Blood Cells Mol Dis. 2005]
Clinical and molecular evaluation of non-dominant hereditary spherocytosis.
Br J Haematol. 2001 Jan; 112(1):42-7.

[Br J Haematol. 2001]
High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis.
J Pediatr. 1998 Jan; 132(1):117-20.

[J Pediatr. 1998]
Review[Characteristics of hereditary spherocytosis]
Nippon Naika Gakkai Zasshi. 1999 Sep 10; 88(9):1825-33.

[Nippon Naika Gakkai Zasshi. 1999]
Review[Molecular aspects of erythrocyte membrane disorders]
Rev Assoc Med Bras. 1994 Jul-Sep; 40(3):216-24.

[Rev Assoc Med Bras. 1994]
» See reviews... | » See all...

betaIV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the central and peripheral nervous system.
Berghs S, Aggujaro D, Dirkx R Jr, Maksimova E, Stabach P, Hermel JM, Zhang JP, Philbrick W, Slepnev V, Ort T, et al. J Cell Biol. 2000 Nov 27; 151(5):985-1002.

[J Cell Biol. 2000]

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