Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15

Research output: Contribution to journalJournal articleResearchpeer-review

Original languageEnglish
Article number532291
JournalFrontiers in Molecular Neuroscience
Volume14
Number of pages12
ISSN1662-5099
DOIs
Publication statusPublished - 2021

ID: 260603824