Your browser doesn't support javascript.
loading
RYR1 and CACNA1S genetic variants identified with statin-associated muscle symptoms.
Isackson, Paul J; Wang, Jianxin; Zia, Mohammad; Spurgeon, Paul; Levesque, Adrian; Bard, Jonathan; James, Smitha; Nowak, Norma; Lee, Tae Keun; Vladutiu, Georgirene D.
Afiliación
  • Isackson PJ; Department of Pediatrics, State University of New York at Buffalo, NY 14203, USA.
  • Wang J; Center for Computational Research, State University of New York at Buffalo, NY 14203, USA.
  • Zia M; Center for Computational Research, State University of New York at Buffalo, NY 14203, USA.
  • Spurgeon P; Center for Computational Research, State University of New York at Buffalo, NY 14203, USA.
  • Levesque A; Center for Computational Research, State University of New York at Buffalo, NY 14203, USA.
  • Bard J; Center for Computational Research, State University of New York at Buffalo, NY 14203, USA.
  • James S; New York State Center of Excellence in Bioinformatics & Life Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA.
  • Nowak N; New York State Center of Excellence in Bioinformatics & Life Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA.
  • Lee TK; Department of Biochemistry, Jacobs School of Medicine & Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA.
  • Vladutiu GD; Department of Pediatrics, State University of New York at Buffalo, NY 14203, USA.
Pharmacogenomics ; 19(16): 1235-1249, 2018 11.
Article en En | MEDLINE | ID: mdl-30325262
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Canales de Calcio / Inhibidores de Hidroximetilglutaril-CoA Reductasas / Canal Liberador de Calcio Receptor de Rianodina / Predisposición Genética a la Enfermedad / Enfermedades Musculares Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Pharmacogenomics Asunto de la revista: FARMACOLOGIA / GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Canales de Calcio / Inhibidores de Hidroximetilglutaril-CoA Reductasas / Canal Liberador de Calcio Receptor de Rianodina / Predisposición Genética a la Enfermedad / Enfermedades Musculares Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Pharmacogenomics Asunto de la revista: FARMACOLOGIA / GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos