Novel exon 2 spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct spectrin defects-Reference-Cited by-同舟云学术

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Novel exon 2 spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct spectrin defects

Published:2013-09-27 Issue:12 Volume:98 Page:1972-1979
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Swierczek S.,Agarwal A. M.,Naidoo K.,Lorenzo F. R.,Whisenant J.,Nussenzveig R. H.,Agarwal N.,Coetzer T. L.,Prchal J. T.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Neonatal Erythrocyte Disorders;Avery's Diseases of the Newborn;2018

2. Three Novel Spectrin Variants in Jaundiced Neonates;Clinical Pediatrics;2017-01-15

3. Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus;Haematologica;2014-06-03

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