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Sequencing for LIPA mutations in patients with a clinical diagnosis of familial hypercholesterolemia.
Sjouke, Barbara; Defesche, Joep C; de Randamie, Janine S E; Wiegman, Albert; Fouchier, Sigrid W; Hovingh, G Kees.
Afiliación
  • Sjouke B; Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands. Electronic address: b.sjouke@amc.uva.nl.
  • Defesche JC; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.
  • de Randamie JSE; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.
  • Wiegman A; Department of Pediatrics, Academic Medical Center, Amsterdam, The Netherlands.
  • Fouchier SW; Department of Medical Biochemistry, Academic Medical Center, Amsterdam, The Netherlands.
  • Hovingh GK; Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands.
Atherosclerosis ; 251: 263-265, 2016 08.
Article en En | MEDLINE | ID: mdl-27423329
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Wolman / Esterol Esterasa / Hiperlipoproteinemia Tipo II / Mutación Tipo de estudio: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Atherosclerosis Año: 2016 Tipo del documento: Article Pais de publicación: Irlanda
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Wolman / Esterol Esterasa / Hiperlipoproteinemia Tipo II / Mutación Tipo de estudio: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Atherosclerosis Año: 2016 Tipo del documento: Article Pais de publicación: Irlanda