Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence o...
Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin
About this item
Full title
Author / Creator
Publisher
Berlin/Heidelberg: Springer-Verlag
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer-Verlag
Subjects
More information
Scope and Contents
Contents
Hereditary persistence of fetal hemoglobin (HPFH) is a rare hereditary condition resulting in elevated levels of fetal hemoglobin (HbF) in adults. Typical HPFH is associated with promoter mutations or large deletions affecting the human fetal globin (
HBG1
and
HBG2
) genes, while genetic defects in other genes involved in human erythrop...
Alternative Titles
Full title
Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_1273209504
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1273209504
Other Identifiers
ISSN
0939-5555
E-ISSN
1432-0584
DOI
10.1007/s00277-012-1625-9
