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Orthopaedic interventions in occipital horn syndrome: a rare case of mutation in ATP7A gene | Egyptian Journal of Medical Human Genetics | Full Text
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Occipital Horn Syndrome Case Report: Multidisciplinary Approach of a Rare Entity | Mendes-Pinto | Journal of Medical Cases
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Time-of-flight imaging in a 4-year-old boy with occipital horn syndrome... | Download Scientific Diagram
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A novel nonsense ATP7A pathogenic variant in a family exhibiting a variable occipital horn syndrome phenotype - ScienceDirect
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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 - Frontiers
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Differences in ATP7A gene expression underlie intrafamilial variability in Menkes disease/occipital horn syndrome | Journal of Medical Genetics
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Occipital Horn Syndrome Case Report: Multidisciplinary Approach of a Rare Entity | Mendes-Pinto | Journal of Medical Cases
USMLE Step 1 & Step 2 CK Tutoring - Egeriausmle - So the right answer is Menkes disease or Kinky Hair syndrome Menkes syndrome is a disorder that affects copper levels in
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