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Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.
Hytönen MK, Arumilli M, Lappalainen AK, Owczarek-Lipska M, Jagannathan V, Hundi S, Salmela E, Venta P, Sarkiala E, Jokinen T, Gorgas D, Kere J, Nieminen P, Drögemüller C, Lohi H. Hytönen MK, et al. PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May. PLoS Genet. 2016. PMID: 27187611 Free PMC article.
A large animal model for CNGB1 autosomal recessive retinitis pigmentosa.
Winkler PA, Ekenstedt KJ, Occelli LM, Frattaroli AV, Bartoe JT, Venta PJ, Petersen-Jones SM. Winkler PA, et al. Among authors: venta pj. PLoS One. 2013 Aug 19;8(8):e72229. doi: 10.1371/journal.pone.0072229. eCollection 2013. PLoS One. 2013. PMID: 23977260 Free PMC article.
93 results