Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 244 for mg
  1. SLC25A24 gene 
    ... cells. This protein is known as an ATP-Mg/Pi carrier because it transports energy molecules called ATP that are attached (bound) to magnesium (Mg) atoms through the mitochondria inner membrane in exchange ...
    https://medlineplus.gov/genetics/gene/slc25a24 - Genetics
  2. Myasthenia gravis 
    ... autoimmune disorders, but the inheritance pattern is unknown. MG Genetic Testing Registry: Myasthenia gravis Myasthenia gravis National ... ClinicalTrials.gov MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE MYASTHENIA GRAVIS; MG MYASTHENIA GRAVIS WITH THYMUS HYPERPLASIA PubMed Angelini C. ...
    https://medlineplus.gov/genetics/condition/myasthenia-gravis - Genetics
  3. VCP gene 
    ... Tooth disease More About This Health Condition 15S Mg(2+)-ATPase p97 subunit CDC48 IBMPFD MGC131997 MGC148092 ...
    https://medlineplus.gov/genetics/gene/vcp - Genetics
  4. 3-methylglutaconyl-CoA hydratase deficiency 
    ... the condition. 3-methylglutaconic aciduria, type I 3-MG-CoA-hydratase deficiency AUH defect MGA, type I ...
    https://medlineplus.gov/...methylglutaconyl-coa-hydratase-deficiency - Genetics
  5. TRPM6 gene 
    The TRPM6 gene provides instructions for making a protein that acts as a channel, which allows charged atoms (ions) of magnesium (Mg2+) to flow into cells; ...
    https://medlineplus.gov/genetics/gene/trpm6 - Genetics
  6. MAGT1 gene 
    The MAGT1 gene provides instructions for making a protein called a magnesium transporter, which moves charged atoms (ions) of magnesium (Mg2+) into certain ...
    https://medlineplus.gov/genetics/gene/magt1 - Genetics
  7. X-linked infantile nystagmus 
    ... G, Pani P, Varma G, Gottlob I, Thomas MG. Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A ... PubMed or Free article on PubMed Central Thomas MG, Crosier M, Lindsay S, Kumar A, Araki M, ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  8. Chromosome 15 
    ... Free article on PubMed Central Bittel DC, Butler MG. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular ... PubMed Bittel DC, Kibiryeva N, Talebizadeh Z, Butler MG. Microarray analysis of gene/transcript expression in Prader- ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  9. KCNA1 gene 
    ... R, Avoni P, McWilliam RC, Stephenson JB, Hanna MG, Kullmann DM, Spauschus A. Clinical, genetic, and expression ... PubMed Jen JC, Graves TD, Hess EJ, Hanna MG, Griggs RC, Baloh RW; CINCH investigators. Primary episodic ...
    https://medlineplus.gov/genetics/gene/kcna1 - Genetics
  10. CARD9 gene 
    ... Delsing CE, Bleeker-Rovers CP, Kullberg BJ, Netea MG. Treatment of candidiasis: insights from host genetics. Expert ... G, Chretien F, Darazam IA, Schaffer AA, Netea MG, De Bruycker JJ, Bernard L, Reynes J, Amazrine ...
    https://medlineplus.gov/genetics/gene/card9 - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next