The association of TMPRSS6 gene polymorphism with iron status in Egyptian children (a pilot study)

Several studies have shown association of single nucleotide polymorphisms (SNPs) of hepcidin regulatory pathways genes with impaired iron status. The most common is in the TMPRSS6 gene. In Africa, very few studie...

Source: BMC Pediatrics - February 10, 2024 Category: Pediatrics Authors: Hanan M. Hamed, Eman El Bostany, Ayat A. Motawie, Amany M. Abd Al-Aziz, Abbass A. Mourad, Hassan M. Salama, Solaf Kamel, Eman M. Hassan, Neveen A. Helmy, Gamila S. El-saeed and Eman A. Elghoroury Tags: Research Source Type: research