Acta Scientific Neurology (ASNE) (ISSN: 2582-1121)

Editorial Volume 7 Issue 5

Study of Hemochromosis and its Cure

Kunal Joon*

Noida International Institute of Medical Sciences, Haryana, India

*Corresponding Author: Kunal Joon, Noida International Institute of Medical Sciences, Haryana, India.

Received: March 21, 2024; Published: April 01, 2024

Abstract

Hemochromosis are inherited disorders resulting in mutation of gene involved in regulating iron metabolism. Studies of HFEC282Y.

Homozygousity this genotype was associated with elevation of serum and transferrin saturation and with iron stores more than 4 grams in females.

 Keywords: Genetics; Genome; Homozygous; Hemochromosis; HFEC282Y; Mutation

References

  1. https://pubmed.ncbi.nlm.nih.gov/15175440/
  2. https://pubmed.ncbi.nlm.nih.gov/11020008/
  3. https://pubmed.ncbi.nlm.nih.gov/10090890/
  4. https://pubmed.ncbi.nlm.nih.gov/10953959/
  5. https://pubmed.ncbi.nlm.nih.gov/17061732/
  6. https://pubmed.ncbi.nlm.nih.gov/8696333/
  7. https://pubmed.ncbi.nlm.nih.gov/11479183/
  8. https://pubmed.ncbi.nlm.nih.gov/16030190/
  9. https://pubmed.ncbi.nlm.nih.gov/19383972/
  10. https://pubmed.ncbi.nlm.nih.gov/16893896/

Citation

Citation: Kunal Joon. “Study of Hemochromosis and its Cure”. Acta Scientific Neurology 7.5 (2024): 01-03.

Copyright

Copyright: © 2024 Kunal Joon. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.




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