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A predominant cardiac phenotype of Anderson-Fabry disease in presence of a MYBPC3 gene mutation and a LAMA4 gene mutation.
Laenens, Dorien; Koopman, Pieter; Cools, Thijs.
Affiliation
  • Laenens D; a Department of Cardiology , Jessa Hospital , Hasselt , Belgium.
  • Koopman P; a Department of Cardiology , Jessa Hospital , Hasselt , Belgium.
  • Cools T; a Department of Cardiology , Jessa Hospital , Hasselt , Belgium.
Acta Cardiol ; 74(1): 84-85, 2019 Feb.
Article in En | MEDLINE | ID: mdl-29415625
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / DNA / Carrier Proteins / Laminin / Fabry Disease / Heart Ventricles / Mutation Type of study: Etiology_studies Limits: Humans / Male / Middle aged Language: En Journal: Acta Cardiol Year: 2019 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiomyopathy, Hypertrophic / DNA / Carrier Proteins / Laminin / Fabry Disease / Heart Ventricles / Mutation Type of study: Etiology_studies Limits: Humans / Male / Middle aged Language: En Journal: Acta Cardiol Year: 2019 Document type: Article Affiliation country: Country of publication: