HEREDITARY HEMOLYTIC ANEMIA β -THALASSEMIA

dc.contributor.authorSaidova Sevinch Odiljon qizi
dc.contributor.authorRasulova Dilnoza Muzaffar qizi
dc.date.accessioned2025-12-29T17:56:50Z
dc.date.issued2024-12-09
dc.description.abstractHereditary hemolytic anemia and beta-thalassemia are blood disorders that affect the process of hemoglobin production in the human body. These diseases are mainly related to genetic factors, and their prevalence and appearance depend on many factors. In this article, we will review the biological basis, clinical manifestations, diagnosis and treatment methods of these diseases.
dc.formatapplication/pdf
dc.identifier.urihttps://webofjournals.com/index.php/5/article/view/2407
dc.identifier.urihttps://asianeducationindex.com/handle/123456789/24196
dc.language.isoeng
dc.publisherWeb of Journals Publishing
dc.relationhttps://webofjournals.com/index.php/5/article/view/2407/2385
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.sourceWeb of Medicine: Journal of Medicine, Practice and Nursing ; Vol. 2 No. 12 (2024): WOM; 41-43
dc.source2938-3765
dc.subjectHereditary hemolytic anemia, blood, thalassemia, clinical environment, treatment, diagnosis, anemia.
dc.titleHEREDITARY HEMOLYTIC ANEMIA β -THALASSEMIA
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typePeer-reviewed Article

item.page.files

item.page.filesection.original.bundle

pagination.showing.labelpagination.showing.detail
loading.default
thumbnail.default.alt
item.page.filesection.name
qizi_2024_hereditary_hemolytic_anemia_-thalassemia.pdf
item.page.filesection.size
215.12 KB
item.page.filesection.format
Adobe Portable Document Format

item.page.collections