載入...

A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis

Defects in erythrocyte ankyrin are the most common cause of typical, dominant hereditary spherocytosis (HS). Detection of ankyrin gene mutations has been complicated by allelic heterogeneity, large gene size, frequent de novo mutations, and associated mRNA instability. Using denaturing high-performa...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Edelman, E. Jennifer, Maksimova, Yelena, Duru, Feride, Altay, Cigdem, Gallagher, Patrick G.
格式: Artigo
語言:Inglês
出版: American Society of Hematology 2007
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1890827/
https://ncbi.nlm.nih.gov/pubmed/17327413
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2006-09-046573
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!