Hematologically Important Mutations: Spectrin Variants in Hereditary Elliptocytosis and Hereditary Pyropoikilocytosis-Reference-Cited by-同舟云学术

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Hematologically Important Mutations: Spectrin Variants in Hereditary Elliptocytosis and Hereditary Pyropoikilocytosis

Published:1996-12 Issue:3 Volume:22 Page:254-258
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Gallagher Patrick G.,Forget Bernard G.

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference44 articles.

1. Disorders of the red cell membrane;Lux,1996

2. Disorders of the red cell membrane skeleton: Hereditary spherocytosis and hereditary elliptocytosis;Becker,1995

3. Spectrin genes in health and disease;Gallagher;Semin Hematol,1993

4. Erythroid and nonerythroid spectrins;Winkelmann;Blood,1993

5. Mutations involving the spectrin heterodimer contact site: Clinical expression and alterations in specific function;Delaunay;Semin Hematol,1993

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2. Anemia at the Extremes of Life: Congenital Hemolytic Anemia;Anemia in the Young and Old;2018-11-14

3. Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China;Annals of Hematology;2018-07-01

4. Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis;Science China Life Sciences;2018-03-19

5. Novel compound heterozygous SPTA1 mutations in a patient with hereditary elliptocytosis;Molecular Medicine Reports;2018-02-26

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