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NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia.
Anderegg, Linda; Im Hof Gut, Michelle; Hetzel, Udo; Howerth, Elizabeth W; Leuthard, Fabienne; Kyöstilä, Kaisa; Lohi, Hannes; Pettitt, Louise; Mellersh, Cathryn; Minor, Katie M; Mickelson, James R; Batcher, Kevin; Bannasch, Danika; Jagannathan, Vidhya; Leeb, Tosso.
Afiliación
  • Anderegg L; Institute of Genetics, Vetsuisse Faculty, University of Bern,Bern, Switzerland.
  • Im Hof Gut M; Kleintierpraxis Laupeneck, Bern, Switzerland.
  • Hetzel U; Institute of Veterinary Pathology, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.
  • Howerth EW; Department of Pathology, College of Veterinary Medicine, University of Georgia, Athens GA, United States of America.
  • Leuthard F; Institute of Genetics, Vetsuisse Faculty, University of Bern,Bern, Switzerland.
  • Kyöstilä K; Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
  • Lohi H; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
  • Pettitt L; Folkhälsan Research Center, Helsinki, Finland.
  • Mellersh C; Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
  • Minor KM; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
  • Mickelson JR; Folkhälsan Research Center, Helsinki, Finland.
  • Batcher K; Kennel Club Genetics Centre, Animal Health Trust, Newmarket, Suffolk CB UU, United Kingdom.
  • Bannasch D; Kennel Club Genetics Centre, Animal Health Trust, Newmarket, Suffolk CB UU, United Kingdom.
  • Jagannathan V; Department of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, MN, United States of America.
  • Leeb T; Department of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, MN, United States of America.
PLoS Genet ; 15(9): e1008378, 2019 09.
Article en En | MEDLINE | ID: mdl-31479451
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de la Motilidad Ciliar / Nucleósido Difosfato Quinasas NM23 Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2019 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de la Motilidad Ciliar / Nucleósido Difosfato Quinasas NM23 Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2019 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Estados Unidos