In-silico Molecular Analysis of Mutated Sequences of HFE1, HFE2, TFR2 and SLC40A1 causing Hemochromatosis Disease
Hemochromatosis is a disorder in iron metabolism that is characterized by excess iron absorption. There are two forms of hemochromatosis: primary hemochromatosis is caused by a problem with your genes. Secondary or acquired hemochromatosis can be caused by other diseases. The main objective of this...
Main Authors: | Bilal Hussain, Hassan Tariq, Tayyaba Sultana, Shahid Mahboob, Tariq Niaz |
---|---|
Format: | Article |
Language: | English |
Published: |
Bulgarian Academy of Sciences
2011-05-01
|
Series: | International Journal Bioautomation |
Subjects: | |
Online Access: | http://www.clbme.bas.bg/bioautomation/2011/vol_15.1/files/15.1_06.pdf |
Similar Items
-
New Mutations in <i>HFE2</i> and <i>TFR2</i> Genes Causing Non <i>HFE</i>-Related Hereditary Hemochromatosis
by: Gonzalo Hernández, et al.
Published: (2021-12-01) -
Non-HFE hemochromatosis
by: Paulo Caleb Júnior de Lima Santos, et al.
Published: (2012-01-01) -
Mutations in HFE and TFR2 genes in a Spanish patient with hemochromatosis Mutaciones en los genes HFE y TFR2 en un paciente español con hemocromatosis
by: Alejandro del-Castillo-Rueda, et al.
Published: (2011-07-01) -
Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis
by: Paulo Lisboa Bittencourt, et al.
Published: (2009-01-01) -
HFE hemochromatosis: an overview about therapeutic recommendations
by: Rodolfo D. Cancado, et al.
Published: (2022-01-01)