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Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense Mutation.
Chowdhury, Rajib; Ashraf, Hassan; Melanson, Michelle; Tanada, Yohei; Nguyen, Minh; Silberbach, Michael; Wakimoto, Hiroko; Benson, D Woodrow; Anderson, Robert H; Kasahara, Hideko.
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  • Chowdhury R; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Ashraf H; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Melanson M; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Tanada Y; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Nguyen M; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Silberbach M; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Wakimoto H; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Benson DW; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Anderson RH; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
  • Kasahara H; From the Department of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville (R.C., H.A., M.M., Y.T., M.N., H.K.); Department of Pediatrics, Oregon Health Science School, Portland (M.S.); Department of Genetics, Harvard Medical School, Boston, MA (H.W.); Departm
Circ Arrhythm Electrophysiol ; 8(5): 1255-64, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26226998
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Mutación Missense / Modelos Animales de Enfermedad / Bloqueo Atrioventricular / Cardiopatías Congénitas Tipo de estudio: Prognostic_studies Idioma: En Revista: Circ Arrhythm Electrophysiol Año: 2015 Tipo del documento: Article
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Mutación Missense / Modelos Animales de Enfermedad / Bloqueo Atrioventricular / Cardiopatías Congénitas Tipo de estudio: Prognostic_studies Idioma: En Revista: Circ Arrhythm Electrophysiol Año: 2015 Tipo del documento: Article