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HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathy.
Millat, Gilles; Janin, Alexandre; de Tauriac, Olivier; Roux, Antoine; Dauphin, Claire.
Affiliation
  • Millat G; Laboratoire de Cardiogénétique Moléculaire, Hospices Civils de Lyon, Lyon, France; NGS Sequencing Platform for Molecular Diagnosis, Hospices Civils de Lyon, Lyon, France; Université de Lyon, Lyon F-69003, France. Electronic address: gilles.millat@chu-lyon.fr.
  • Janin A; Laboratoire de Cardiogénétique Moléculaire, Hospices Civils de Lyon, Lyon, France; NGS Sequencing Platform for Molecular Diagnosis, Hospices Civils de Lyon, Lyon, France; Université de Lyon, Lyon F-69003, France.
  • de Tauriac O; Service de Cardiologie, Centre Hospitalier Emile Roux, Le Puy, France.
  • Roux A; Service de Cardiologie, Centre Hospitalier Gabriel-Montpied, Clermont-Ferrand, France.
  • Dauphin C; Service de Cardiologie, Centre Hospitalier Gabriel-Montpied, Clermont-Ferrand, France.
Eur J Med Genet ; 58(9): 439-42, 2015 Sep.
Article in En | MEDLINE | ID: mdl-26206080
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bradycardia / Potassium Channels / Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels / Muscle Proteins / Cardiomyopathies Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Female / Humans Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Country of publication: Netherlands
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bradycardia / Potassium Channels / Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels / Muscle Proteins / Cardiomyopathies Type of study: Prognostic_studies Limits: Adolescent / Adult / Child / Female / Humans Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Country of publication: Netherlands