Rare diseases are rare, but
rare disease patients are numerous

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• • CANADA
  • Colombie-Britannique
  • VANCOUVER
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of British Columbia
  • Faculty of Medicine
  • More details
• • CANADA
  • Ontario
  • OTTAWA, ONTARIO
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of Ottawa
  • Faculty of Medicine -
  • More details
• • CANADA
  • Québec
  • MONTREAL
  • FORGE - Finding of Rare Disease Genes in Canada
  • Centre hospitalier universitaire Sainte-Justine
  • Pédiatrie
  • More details
• • FRANCE
  • PAYS DE LA LOIRE
  • NANTES
  • Genetics of congenital cardiac conduction defects
  • CHU de Nantes - Hôpital Nord Guillaume et René Laënnec
  • Clinique cardiologique et maladies vasculaires
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• • FRANCE
  • PAYS DE LA LOIRE
  • NANTES
  • Phenotype profile of congenital cardiac conduction defects
  • CHU de Nantes - Hôpital Nord Guillaume et René Laënnec
  • Clinique cardiologique et maladies vasculaires
  • More details
• • GERMANY
  • Baden-Württemberg
  • ULM
  • Excitation-contraction coupling in health and disease: Ion channel diseases - diagnosis, pathogenesis and therapy
  • Universität Ulm
  • Institut für Angewandte Physiologie
  • More details
• • GERMANY
  • Hessen
  • MARBURG
  • Structure and function of potassium channels of the K2P family in the cardiovascular system (FOR1086)
  • Philipps-Universität Marburg
  • AG Zellphysiologie (Prof. Dr. Dr. Daut)
  • More details
• • GERMANY
  • Nordrhein-Westfalen
  • MÜNSTER
  • Genetic variants in K2P channel genes and monogenetic cardial conduction defects (FOR1086)
  • Universitätsklinikum Münster
  • Institut für Genetik von Herzerkrankungen
  • More details
• • ITALY
  • LAZIO
  • ROMA
  • Molecular basis of conduction defects of the heart
  • Istituto CSS-Mendel
  • Laboratorio di Biologia Molecolare e Citogenetica
  • More details
• • ITALY
  • PUGLIA
  • BARI
  • Hereditary chloride channelopathies of skeletal muscle and kidney: from genotype to phenotype and novel pharmacotherapeutical approaches
  • Università degli Studi di Bari
  • Sezione di Farmacologia
  • More details
• • LEBANON
  • Beyrouth
  • BEIRUT
  • Genetic causes of congenital heart diseases in the Lebanese population: screening for mutations in transcription factors implicated in heart development and cardiac function
  • American University of Beirut
  • Département de biochimie
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• • SWITZERLAND
  • Suisse Alémanique
  • BASEL
  • Genotyping of patients with inherited arrythmias and cardiomyopathies
  • Universitätsspital Basel
  • CardioBiology Research Laboratories
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• • UNITED KINGDOM
  • Greater London
  • LONDON
  • Gene identification in inherited cardiovascular disease
  • The Heart Hospital
  • Centre for Cardiology In The Young
  • More details