A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiency

author
created [InstanceEdit:9957526] Rothfels, Karen, 2025-06-18
dbId 9957527
displayName A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiency
journal J Inherit Metab Dis
pages 356-7
pubMedIdentifier 7474905
schemaClass LiteratureReference
title A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiency
url http://www.ncbi.nlm.nih.gov/pubmed/7474905
volume 18
year 1995
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