Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15
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- Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15
Final published version, 2.11 MB, PDF document
Original language | English |
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Article number | 532291 |
Journal | Frontiers in Molecular Neuroscience |
Volume | 14 |
Number of pages | 12 |
ISSN | 1662-5099 |
DOIs | |
Publication status | Published - 2021 |
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ID: 260603824