Protein 4.1 Lille, a novel mutation in the downstream initiation codon of protein 4.1 gene associated with heterozygous 4,1(−) hereditary elliptocytosis
- 1 January 1995
- journal article
- mutation in-brief
- Published by Hindawi Limited in Human Mutation
- Vol. 5 (4) , 339-340
- https://doi.org/10.1002/humu.1380050412
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact siteBlood, 1994
- Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene.Journal of Clinical Investigation, 1992
- Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern AlpsBlood, 1991
- Primer-directed enzymatic amplification of DNA with a thermostable DNA polymeraseScience, 1988
- The heterozygous form of 4.1(-) hereditary elliptocytosis [the 4.1(-) trait]Blood, 1985