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Results 1 - 4 of 4 for CALCIUM CATION OR CYANOCOBALAMIN OR FOLIC ACID OR PYRIDOXINE
  1. Hereditary folate malabsorption 
    ... Congenital defect of folate absorption Congenital folate malabsorption Folic acid transport defect Genetic Testing Registry: Congenital defect of ... K, Dlamini JC, Ivashkin V. The Concept of Folic Acid in Health and Disease. Molecules. 2021 Jun 18; ...
    https://medlineplus.gov/.../hereditary-folate-malabsorption - Genetics
  2. TRPM4 gene 
    ... about Brugada syndrome More About This Health Condition calcium-activated non-selective cation channel 1 hTRPM4 long transient receptor potential channel ...
    https://medlineplus.gov/genetics/gene/trpm4 - Genetics
  3. TRPV4 gene 
    ... these mutations change single protein building blocks (amino acids) in the TRPV4 calcium channel. However, a few mutations insert or delete ... these skeletal and neurological disorders change single amino acids in the TRPV4 calcium channel. These mutations likely result in an overactive ...
    https://medlineplus.gov/genetics/gene/trpv4 - Genetics
  4. TRPM1 gene 
    ... for making a protein called transient receptor potential cation channel subfamily M member 1 (TRPM1). This protein acts as a channel, transporting positively charged atoms (cations) into cells. The TRPM1 channel is found on ...
    https://medlineplus.gov/genetics/gene/trpm1 - Genetics