Item talk:Q167689

{

 "OpenAlex": {
   "display_name": "Metabolic Disorders and Biochemical Genetics",
   "description": "This cluster of papers covers a wide range of topics related to metabolic disorders and biochemical genetics, including newborn screening, mitochondrial function, carnitine metabolism, phenylketonuria, tandem mass spectrometry, inborn errors of metabolism, tyrosine hydroxylase activity, and tetrahydrobiopterin biosynthesis. The papers discuss various aspects of diagnosis, management, and treatment of these disorders.",
   "keywords": [
     "Metabolic Disorders",
     "Biochemical Genetics",
     "Newborn Screening",
     "Mitochondrial Function",
     "Carnitine",
     "Phenylketonuria",
     "Tandem Mass Spectrometry",
     "Inborn Errors of Metabolism",
     "Tyrosine Hydroxylase",
     "Tetrahydrobiopterin"
   ],
   "ids": {
     "openalex": "https://openalex.org/T11027",
     "wikipedia": "https://en.wikipedia.org/wiki/Metabolic_disorder"
   },
   "subfield": {
     "id": "https://openalex.org/subfields/1308",
     "display_name": "Clinical Biochemistry"
   },
   "field": {
     "id": "https://openalex.org/fields/13",
     "display_name": "Biochemistry, Genetics and Molecular Biology"
   },
   "domain": {
     "id": "https://openalex.org/domains/1",
     "display_name": "Life Sciences"
   },
   "updated_date": "2024-08-12T05:37:41.053904",
   "created_date": "2024-01-23",
   "type": "topic",
   "oa_id": "T11027",
   "id": "https://openalex.org/T11027"
 }

}