Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutations

author
created [InstanceEdit:9957611] Rothfels, Karen, 2025-06-18
dbId 9957610
displayName Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutations
journal J Inherit Metab Dis
pages 669-76
pubMedIdentifier 11117428
schemaClass LiteratureReference
title Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutations
url http://www.ncbi.nlm.nih.gov/pubmed/11117428
volume 23
year 2000
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