The Spectrum of SPTA1-Associated Hereditary Spherocytosis-Reference-Cited by-同舟云学术

The Spectrum of SPTA1-Associated Hereditary Spherocytosis

Published:2019-07-03 Issue: Volume:10 Page:
ISSN:1664-042X
Container-title:Frontiers in Physiology
language:
Short-container-title:Front. Physiol.

Author:

Chonat Satheesh,Risinger Mary,Sakthivel Haripriya,Niss Omar,Rothman Jennifer A.,Hsieh Loan,Chou Stella T.,Kwiatkowski Janet L.,Khandros Eugene,Gorman Matthew F.,Wells Donald T.,Maghathe Tamara,Dagaonkar Neha,Seu Katie G.,Zhang Kejian,Zhang Wenying,Kalfa Theodosia A.

Funder

National Institutes of Health

Publisher

Frontiers Media SA

Subject

Physiology (medical),Physiology

Reference19 articles.

1. Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.;Agre;Nature,1985

2. Deficient red-cell spectrin in severe, recessively inherited spherocytosis.;Agre;N. Engl. J. Med.,1982

3. Proteins involved in membrane–cytoskeleton association in human erythrocytes: spectrin, ankyrin, and band 3.;Bennett;Meth. Enzymol.,1983

4. Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus.;Bogardus;Haematologica,2014

5. Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenance.;Clark;Blood,1983

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