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...

詳細記述

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書誌詳細
出版年:PLoS Genet
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2016
主題:
Research Article
オンライン･アクセス: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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