The Significance of the 187G (H63D) Mutation in Hemochromatosis

American Journal of Human Genetics - United States
doi 10.1016/s0002-9297(07)64339-0
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Elsevier BV

Related search

The Role of Hemochromatosis C282Y and H63D Mutations in the Development of Type 2 Diabetes Mellitus in Greece

Hormones
MedicineEndocrinologyMetabolismDiabetes
2003English

Major Histocompatibility Complex Class I Associations in Iron Overload: Evidence for a New Link Between the HFE H63D Mutation, HLA-A29, and Non-Classical Forms of Hemochromatosis

Immunogenetics
ImmunologyGenetics
1998English

Idiopathic Hemochromatosis With the Mutation of Ala176Val Heterozygous for HFE Gene.

Internal Medicine
Internal MedicineMedicine
2001English

The Heart in Hemochromatosis

Diabetes
Internal MedicineEndocrinologyMetabolismDiabetes
1953English

Clinical Significance of Prothrombin G20210A Mutation in Homozygous Patients

American Journal of Hematology
Hematology
2017English

A Novel Rat Model of Hereditary Hemochromatosis Due to a Mutation in Transferrin Receptor 2

Blood
BiochemistryImmunologyCell BiologyHematology
2012English

Hemochromatosis

JAMA - Journal of the American Medical Association
Medicine
1978English

EGFR Mutation: Significance as a Stratification Factor in the Era of Molecular-Targeted Therapy

Oncology Letters
Cancer ResearchOncology
2011English

The Molecular Basis of Ferroportin-Linked Hemochromatosis

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2005English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy