Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report. Issue 12 (12th July 2020)
- Record Type:
- Journal Article
- Title:
- Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report. Issue 12 (12th July 2020)
- Main Title:
- Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
- Authors:
- Pokhrel, Nishan Babu
Khanal, Shambhu
Chapagain, Parikshit
Pokhrel, Biraj
Shrestha, Anjan - Abstract:
- Abstract: β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation. Abstract : β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.
- Is Part Of:
- Clinical case reports. Volume 8:Issue 12(2020)
- Journal:
- Clinical case reports
- Issue:
- Volume 8:Issue 12(2020)
- Issue Display:
- Volume 8, Issue 12 (2020)
- Year:
- 2020
- Volume:
- 8
- Issue:
- 12
- Issue Sort Value:
- 2020-0008-0012-0000
- Page Start:
- 2341
- Page End:
- 2345
- Publication Date:
- 2020-07-12
- Subjects:
- anemia -- h63d mutation -- hereditary hemochromatosis -- HFE gene -- iron overload -- β‐thalassemia
Medicine -- Periodicals
616.09 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2050-0904 ↗ - DOI:
- 10.1002/ccr3.3096 ↗
- Languages:
- English
- ISSNs:
- 2050-0904
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23377.xml