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108 results
  1. OAT gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/oat
    ... PubMed Catalog of Genes and Diseases from OMIM ORNITHINE AMINOTRANSFERASE; OAT Gene and Variant Databases NCBI Gene ClinVar References Mashima YG, Weleber RG, Kennaway NG, Inana G. ...
  2. OTC gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/otc
    ... PubMed Catalog of Genes and Diseases from OMIM ORNITHINE CARBAMOYLTRANSFERASE; OTC Gene and Variant Databases NCBI Gene ClinVar References Ah Mew N, Simpson KL, Gropman AL, Lanpher ...
  3. Ornithine transcarbamylase deficiency: MedlinePlus Genetics 
    https://medlineplus.gov/.../ornithine-transcarbamylase-deficiency
    ... gov Catalog of Genes and Diseases from OMIM ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Scientific Articles on PubMed PubMed References Ah Mew N, Simpson KL, Gropman AL, Lanpher ...
  4. SLC25A15 gene: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/gene/slc25a15
    ... from OMIM SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER, ORNITHINE TRANSPORTER), MEMBER 15; SLC25A15 Gene and Variant Databases NCBI Gene ClinVar References Camacho JA, Mardach R, Rioseco-Camacho N, Ruiz- ...
  5. Gyrate atrophy of the choroid and retina: MedlinePlus Genetics 
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina
    ... AND RETINA; GACR Scientific Articles on PubMed PubMed References Cleary MA, Dorland L, de Koning TJ, Poll-The BT, Duran M, Mandell R, Shih VE, Berger R, Olpin SE, Besley GT. Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentation. J ...
  6. Ornithine translocase deficiency: MedlinePlus Genetics 
    https://medlineplus.gov/.../ornithine-translocase-deficiency
    ... disorders. Learn more about the gene associated with Ornithine translocase deficiency SLC25A15 Inheritance This condition is inherited ...
  7. Mitochondrial Diseases 
    https://medlineplus.gov/mitochondrialdiseases.html
    ... retinitis pigmentosa: MedlinePlus Genetics (National Library of Medicine) ... (National Institutes of Health) Journal Articles References and abstracts from MEDLINE/PubMed (National Library of ...
  8. NLM Digital Collections - The Recombinant DNA Controversy: A Memoir: Science, Politics, and the Public Interest ... 
    Publication: American Society for Microbiology, 2001
    resource.nlm.nih.gov/101584939X188
    ... a University of Penn- sylvania protocol focused on ornithine transcarbamylase (OTC) ... reference to the financial dimension of biomedical re- search ...
  9. Creatine Deficiency Syndromes - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK3794
    ... levels. Treatment of GAMT deficiency requires supplementation of ornithine and dietary restriction of arginine or protein. In ... citrullinemia type 1 ) [ van Spronsen et al 2006 ], ornithine aminotransferase deficiency (gyrate atrophy of the choroid and ...
  10. xmlTopicIndex.xml 
    https://medlineplus.gov/download/TopicIndex.xml
    ... other_name >OKT deficiency</other_name><other_name >Ornithine aminotransferase deficiency</other_name><other_name >Ornithine keto acid aminotransferase deficiency</other_name><other_name > ...
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