Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome.
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| Title: | Characterization of Loss-Of-Function KCNJ2 Mutations in Atypical Andersen Tawil Syndrome. |
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| Authors: | Le Tanno P; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France., Folacci M; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France., Revilloud J; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France., Faivre L; Medical Genetics Department, Dijon Bourgogne University Hospital, François Mitterand Hospital, Dijon, France., Laurent G; Cardiology Department, Dijon Bourgogne University Hospital, François Mitterand Hospital, Dijon, France., Pinson L; Medical Genetics Department, University Hospital, Montpellier, France.; Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Montpellier, France.; Genetic Department for Rare Diseases and Personalized Medicine, Clinical Division, Montpellier, France., Amedro P; Pediatric and Congenital Cardiology Department, Clinical Investigation Centre, PhyMedExp, CNRS, INSERM, University of Montpellier, University Hospital, Montpellier, France., Millat G; Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon, Lyon, France., Janin A; Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon, Lyon, France., Vivaudou M; CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France., Roux-Buisson N; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France., Fauré J; Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France. |
| Source: | Frontiers in genetics [Front Genet] 2021 Nov 25; Vol. 12, pp. 773177. Date of Electronic Publication: 2021 Nov 25 (Print Publication: 2021). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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