Molecular identification of a rare hemoglobin variant, Hb J-Iran [beta77(EF1)His->Asp], in Denizli province of Turkey
Loading...
Date
2006
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Open Access Color
OpenAIRE Downloads
OpenAIRE Views
Abstract
Hb J-Iran [beta77(EF1)His-Asp], a rare hemoglobin variant that does not present health problems, was reported for the first time in the Turkish population in 1986. Our case is the fourth case reported in Turkey and the first case from the Denizli province. © Turkish Society of Hematology.
Description
Keywords
Abnormal hemoglobin, Hb J-Iran, aspartic acid, beta globin, DNA, elongation factor 1, hemoglobin A2, hemoglobin J, histidine, adult, article, blood analysis, case report, column chromatography, DNA sequence, exon, hemoglobin determination, human, male, polymerase chain reaction, screening test, Turkey (republic)
Fields of Science
Citation
WoS Q
Scopus Q
Q3
Source
Turkish Journal of Hematology
Volume
23
Issue
3
Start Page
164
End Page
166
