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Ornithine transcarbamylase deficiency: A diagnostic odyssey.
Knerr, Ina; Cassiman, David.
Affiliation
  • Knerr I; National Centre for Inherited Metabolic Disorders, Children's Health Ireland (CHI) at Temple Street, Dublin, Republic of Ireland.
  • Cassiman D; University College Dublin (UCD), UCD School of Medicine, Dublin, Republic of Ireland.
J Inherit Metab Dis ; 45(4): 661-662, 2022 07.
Article in En | MEDLINE | ID: mdl-35734906
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ornithine Carbamoyltransferase Deficiency Disease Type of study: Diagnostic_studies Limits: Humans Language: En Journal: J Inherit Metab Dis Year: 2022 Document type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ornithine Carbamoyltransferase Deficiency Disease Type of study: Diagnostic_studies Limits: Humans Language: En Journal: J Inherit Metab Dis Year: 2022 Document type: Article