Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-...
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes
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United States: Public Library of Science
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English
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United States: Public Library of Science
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One to two percent of all children are born with a developmental disorder requiring pediatric hospital admissions. For many such syndromes, the molecular pathogenesis remains poorly characterized. Parallel developmental disorders in other species could provide complementary models for human rare diseases by uncovering new candidate genes, improving...
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Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes
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TN_cdi_plos_journals_1797506067
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1797506067
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ISSN
1553-7404,1553-7390
E-ISSN
1553-7404
DOI
10.1371/journal.pgen.1006037
