Genetic analysis of TMPRSS6 gene in Saudi female patients with iron deficiency anemia
Author(s) -
Lamiaa H. AlJamea,
Alexander Woodman,
Nihal M. Heiba,
Shereen A. Elshazly,
Noureddine Ben Khalaf,
Dahmani M. Fathallah,
Moudi E. Al-Nashmi,
Jenifer V. Quiambao,
Abdel Halim Salem
Publication year - 2020
Publication title -
hematology/oncology and stem cell therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 22
eISSN - 1658-3876
pISSN - 2589-0646
DOI - 10.1016/j.hemonc.2020.04.007
Subject(s) - tmprss6 , hepcidin , iron deficiency anemia , exon , biology , genetics , gene , untranslated region , allele , anemia , medicine , biochemistry , rna , serine protease , protease , enzyme
Mutations in transmembrane protease serine 6 (TMPRSS6) gene induce high hepcidin level, which causes iron-refractory iron deficiency anemia (IRIDA) by preventing duodenal iron absorption. This study aims to identify the common genetic variations of the TMPRSS6 gene that affect iron levels among Saudi female patients with iron deficiency anemia (IDA).
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