HFE GENE MUTATIONS IN CRYPTOGENIC CIRRHOSIS PATIENTS

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SENDI HOSSEIN; MEHRAB MOHSENI MARJAN

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Hepatitis Monthly Year:2012 | Volume:12 | Issue:1 (42) Page(s): 48-49

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Information Journal Paper

Title

HFE GENE MUTATIONS IN CRYPTOGENIC CIRRHOSIS PATIENTS

Author(s)

SENDI HOSSEIN | MEHRAB MOHSENI MARJAN | Issue Writer Certificate

Keywords

HEMOCHROMATOSIS

IRAN

C282Y

H63D

Abstract

In western countries, HFF-linked hereditary HEMOCHROMATOSIS (HH) is considered to be the most common cause of iron overload.the HFE gene, first identified in 1996, is located on the short arm of chromosome 6. The majority of patients with phenotypic HH are homozygous for the C282Y mutation, a major mutation of the HFE gene, whereas compound heterozygosity (C282Y/H63D) is found in patients with a milder iron loading phenotype (1)...

Cites

HAPLOTYPE ANALYSIS OF HEMOCHROMATOSIS GENE POLYMORPHISMS IN CHRONIC HEPATITIS C VIRUS INFECTION: A CASE CONTROL STUDY

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APA: Copy

SENDI, HOSSEIN, & MEHRAB MOHSENI, MARJAN. (2012). HFE GENE MUTATIONS IN CRYPTOGENIC CIRRHOSIS PATIENTS. HEPATITIS MONTHLY, 12(1 (42)), 48-49. SID. https://sid.ir/paper/306509/en

Vancouver: Copy

SENDI HOSSEIN, MEHRAB MOHSENI MARJAN. HFE GENE MUTATIONS IN CRYPTOGENIC CIRRHOSIS PATIENTS. HEPATITIS MONTHLY[Internet]. 2012;12(1 (42)):48-49. Available from: https://sid.ir/paper/306509/en

IEEE: Copy

HOSSEIN SENDI, and MARJAN MEHRAB MOHSENI, “HFE GENE MUTATIONS IN CRYPTOGENIC CIRRHOSIS PATIENTS,” HEPATITIS MONTHLY, vol. 12, no. 1 (42), pp. 48–49, 2012, [Online]. Available: https://sid.ir/paper/306509/en

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