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Results 1 - 7 of 7 for Disorder of tyrosine metabolism
  1. PCBD1 gene 
    ... or Free article on PubMed Central Longo N. Disorders of biopterin metabolism. J Inherit Metab Dis. 2009 Jun;32(3): ... 32(3):457. Citation on PubMed Shintaku H. Disorders of tetrahydrobiopterin metabolism and their treatment. Curr Drug Metab. 2002 Apr; ...
    https://medlineplus.gov/genetics/gene/pcbd1 - Genetics
  2. PTS gene 
    ... 01)00669-6. Citation on PubMed Longo N. Disorders of biopterin metabolism. J Inherit Metab Dis. 2009 Jun;32(3): ... 32(3):457. Citation on PubMed Shintaku H. Disorders of tetrahydrobiopterin metabolism and their treatment. Curr Drug Metab. 2002 Apr; ...
    https://medlineplus.gov/genetics/gene/pts - Genetics
  3. QDPR gene 
    ... CO;2-C. Citation on PubMed Longo N. Disorders of biopterin metabolism. J Inherit Metab Dis. 2009 Jun;32(3): ... 10.1007/s004390000407. Citation on PubMed Shintaku H. Disorders of tetrahydrobiopterin metabolism and their treatment. Curr Drug Metab. 2002 Apr; ...
    https://medlineplus.gov/genetics/gene/qdpr - Genetics
  4. GCH1 gene 
    ... 0000037349.08483.96. Citation on PubMed Longo N. Disorders of biopterin metabolism. J Inherit Metab Dis. 2009 Jun;32(3): ... 1):1-11. Citation on PubMed Shintaku H. Disorders of tetrahydrobiopterin metabolism and their treatment. Curr Drug Metab. 2002 Apr; ...
    https://medlineplus.gov/genetics/gene/gch1 - Genetics
  5. HFE gene 
    ... Central Nemeth E, Ganz T. Regulation of iron metabolism by hepcidin. Annu Rev Nutr. 2006;26:323-42. doi: 10.1146/annurev.nutr.26.061505.111303. Citation on PubMed Pantopoulos K. Inherited Disorders of Iron Overload. Front Nutr. 2018 Oct 29; ...
    https://medlineplus.gov/genetics/gene/hfe - Genetics
  6. Alkaptonuria 
    ... helps break down the amino acids phenylalanine and tyrosine, which are important building blocks of proteins. Mutations ... homogentisic acid, which is produced as phenylalanine and tyrosine are broken down, accumulates in the body. Excess ...
    https://medlineplus.gov/genetics/condition/alkaptonuria - Genetics
  7. SLC22A5 gene 
    ... on PubMed Tein I. Carnitine transport: pathophysiology and metabolism of known molecular defects. J Inherit Metab Dis. ...
    https://medlineplus.gov/genetics/gene/slc22a5 - Genetics