Research of Hereditary Sideroblastic Anemia has been linked to Sideroblastic Anemia, Anemia, Iron Overload, Ataxia, Genetic Diseases, X-linked. The study of Hereditary Sideroblastic Anemia has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hereditary Sideroblastic Anemia include Transport, Pathogenesis, Translation, Localization, Cell Differentiation. These pathways complement our catalog of research reagents for the study of Hereditary Sideroblastic Anemia including antibodies and ELISA kits against ALAS2, ABCB7, ALAS1, FECH, FXN.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Hereditary Sideroblastic Anemia below!
For more information on how to use Laverne, please read the How to Guide.
We have 563 products for the study of Hereditary Sideroblastic Anemia that can be applied to Western Blot, Flow Cytometry, Immunohistochemistry, Immunocytochemistry/Immunofluorescence from our catalog of antibodies and ELISA kits.
Hereditary Sideroblastic Anemia is also known as Congenital Sideroblastic Anaemia, Congenital Sideroblastic Anemia, Hereditary Sideroblastic Anaemia, X-linked Sideroblastic Anaemia, X-linked Sideroblastic Anemia.
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