Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes

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 dis...

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Détails bibliographiques
Publié dans:PLoS Genet
Auteurs principaux: Hytönen, Marjo K., Arumilli, Meharji, Lappalainen, Anu K., Owczarek-Lipska, Marta, Jagannathan, Vidhya, Hundi, Sruthi, Salmela, Elina, Venta, Patrick, Sarkiala, Eva, Jokinen, Tarja, Gorgas, Daniela, Kere, Juha, Nieminen, Pekka, Drögemüller, Cord, Lohi, Hannes
Format: Artigo
Langue:Inglês
Publié: Public Library of Science 2016
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4871343/
https://ncbi.nlm.nih.gov/pubmed/27187611
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1006037
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