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Results 1 - 10 of 11 for ADENINE OR DEXTROSE
  1. Adenine phosphoribosyltransferase deficiency 
    Adenine phosphoribosyltransferase (APRT) deficiency is an inherited condition that affects the kidneys and urinary tract. The most common feature of this condition ...
    https://medlineplus.gov/...nine-phosphoribosyltransferase-deficiency - Genetics
  2. Progressive external ophthalmoplegia 
    ... Keranen S, Peltonen L, Suomalainen A. Role of adenine nucleotide translocator 1 in mtDNA maintenance. Science. 2000 ... Free article on PubMed Central Sharer JD. The adenine nucleotide translocase type 1 (ANT1): a new factor ...
    https://medlineplus.gov/.../progressive-external-ophthalmoplegia - Genetics
  3. Glycoprotein VI deficiency 
    ... J, Pillois X, Nurden AT, Mezzano D. An adenine insertion in exon 6 of human GP6 generates ...
    https://medlineplus.gov/.../condition/glycoprotein-vi-deficiency - Genetics
  4. Huntington's disease 
    ... a series of three DNA building blocks (cytosine, adenine, and guanine) that appear multiple times in a ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease - Genetics
  5. Dentatorubral-pallidoluysian atrophy 
    ... a series of three DNA building blocks (cytosine, adenine, and guanine) that appear multiple times in a ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
  6. Spinocerebellar ataxia type 3 
    ... a series of three DNA building blocks (cytosine, adenine, and guanine) that appear multiple times in a ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  7. Friedreich ataxia 
    ... three DNA building blocks (one guanine and two adenines) that appear multiple times in a row. Normally, ...
    https://medlineplus.gov/genetics/condition/friedreich-ataxia - Genetics
  8. Riboflavin transporter deficiency neuronopathy 
    ... is the core component of molecules called flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN). FAD and ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  9. Spinocerebellar ataxia type 1 
    ... a series of three DNA building blocks (cytosine, adenine, and guanine) that appear multiple times in a ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  10. Spinocerebellar ataxia type 2 
    ... a series of three DNA building blocks (cytosine, adenine, and guanine) that appear multiple times in a ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
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