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Open Access
Peer-reviewed
Research Article
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes
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Marjo K. Hytönen,
Affiliations Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland, Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland, The Folkhälsan Institute of Genetics, Helsinki, Finland
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Meharji Arumilli,
Affiliations Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland, Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland, The Folkhälsan Institute of Genetics, Helsinki, Finland
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Anu K. Lappalainen,
Affiliation Department of Equine and Small Animal Medicine, University of Helsinki, Helsinki, Finland
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Marta Owczarek-Lipska,
Affiliation Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland
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Vidhya Jagannathan,
Affiliation Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland
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Sruthi Hundi,
Affiliations Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland, Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland, The Folkhälsan Institute of Genetics, Helsinki, Finland
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Elina Salmela,
Affiliations Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland, Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland, The Folkhälsan Institute of Genetics, Helsinki, Finland
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Patrick Venta,
Affiliation Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, United States of America
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Eva Sarkiala,
Affiliation Department of Equine and Small Animal Medicine, University of Helsinki, Helsinki, Finland
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Tarja Jokinen,
Affiliations Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland, Department of Equine and Small Animal Medicine, University of Helsinki, Helsinki, Finland
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Daniela Gorgas,
Affiliation Division of Clinical Radiology, Department of Clinical Veterinary Medicine, Vetsuisse Faculty, University of Bern, Bern, Switzerland
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Juha Kere,
Affiliations Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland, The Folkhälsan Institute of Genetics, Helsinki, Finland, Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden
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Pekka Nieminen,
Affiliation Department of Oral and Maxillofacial Diseases, University of Helsinki, Helsinki, Finland
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Cord Drögemüller ,
Contributed equally to this work with: Cord Drögemüller, Hannes Lohi
Affiliation Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland
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Hannes Lohi
Contributed equally to this work with: Cord Drögemüller, Hannes Lohi
* E-mail: hannes.lohi@helsinki.fi
Affiliations Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland, Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland, The Folkhälsan Institute of Genetics, Helsinki, Finland
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Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes
- Marjo K. Hytönen,
- Meharji Arumilli,
- Anu K. Lappalainen,
- Marta Owczarek-Lipska,
- Vidhya Jagannathan,
- Sruthi Hundi,
- Elina Salmela,
- Patrick Venta,
- Eva Sarkiala,
- Tarja Jokinen
- Published: May 17, 2016
- https://doi.org/10.1371/journal.pgen.1006037