Journal article
Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
Clinical case reports, Vol.8(12), pp.2341-2345
12/2020
DOI: 10.1002/ccr3.3096
PMID: 33363736
Abstract
β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation. β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.
Details
- Title: Subtitle
- Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
- Creators
- Nishan Babu Pokhrel - Tribhuvan UniversityShambhu Khanal - Tribhuvan UniversityParikshit Chapagain - Tribhuvan UniversityBiraj Pokhrel - Tribhuvan UniversityAnjan Shrestha - Tribhuvan University
- Resource Type
- Journal article
- Publication Details
- Clinical case reports, Vol.8(12), pp.2341-2345
- DOI
- 10.1002/ccr3.3096
- PMID
- 33363736
- NLM abbreviation
- Clin Case Rep
- ISSN
- 2050-0904
- eISSN
- 2050-0904
- Publisher
- John Wiley and Sons Inc
- Number of pages
- 5
- Alternative title
- POKHREL et al
- Language
- English
- Date published
- 12/2020
- Academic Unit
- Internal Medicine
- Record Identifier
- 9985177933402771
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