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Primary Hypomagnesemia (disorder): Disease Bioinformatics

Research of Primary Hypomagnesemia (disorder) has been linked to Magnesium Deficiency, Hypocalcemia, Convulsions, Tetany, Malabsorption Syndrome. The study of Primary Hypomagnesemia (disorder) has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Primary Hypomagnesemia (disorder) include Excretion, Transport, Intestinal Absorption, Secretion, Transepithelial Transport. These pathways complement our catalog of research reagents for the study of Primary Hypomagnesemia (disorder) including antibodies and ELISA kits against TRPM6, PTH, CLDN16, TBPL1, TYRP1.

Primary Hypomagnesemia (disorder) Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Primary Hypomagnesemia (disorder) below! For more information on how to use Laverne, please read the How to Guide.

Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 1740 products for the study of Primary Hypomagnesemia (disorder) that can be applied to Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.

Recombinant Human PTRH1 GST (N-Term) Protein

H00138428-P01