Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome-Reference-Cited by-同舟云学术

Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome

Published:2017-12-29 Issue:5 Volume:137 Page:452-461
ISSN:0001-6314
Container-title:Acta Neurologica Scandinavica
language:en
Short-container-title:Acta Neurol Scand

Author:

Witting N.¹^ORCID,Laforêt P.²,Voermans N. C.³,Roux-Buisson N.⁴⁵,Bompaire F.⁶,Rendu J.⁴⁵,Duno M.⁷,Feillet F.⁸,Kamsteeg E.-J.³,Poulsen N. S.¹,Dahlqvist J. R.¹,Romero N. B.⁹,Fauré J.⁴⁵,Vissing J.¹,Behin A.²

Affiliation:

1. Department of Neurology; Copenhagen Neuromuscular Centre; Rigshospitalet; University of Copenhagen; Copenhagen Denmark

2. Centre de Référence de Pathologie Neuromusculaire Paris-Est; Groupe Hospitalier Pitié-Salpêtrière; Institut de Myologie; AP-HP; Paris Cedex France

3. Department of Human Genetics; Radboud University Medical Centre; Nijmegen The Netherlands

4. INSERM U121; Equipe CMyPath; Institut des Neurosciences; Grenoble France

5. Biochimie Génétique et Moléculaire; Institut de Biologie et Pathologie; CHU; Grenoble France

6. Neurologie; Hopital d'instruction des Armées Percy; Clamart France

7. Department of Clinical Genetics; Rigshospitalet; University of Copenhagen; Copenhagen Denmark

8. Service de Médecine Infantile 1; Centre de Référence des Maladies Héréditaires du Métabolisme; Centre Hospitalier Universitaire Brabois-Enfants; Vandœuvre-lès-Nancy France

9. Laboratoire de Pathologie Musculaire Risler; Groupe Hospitalier Pitié-Salpêtrière; Paris France

Funder

Novo Nordisk UK Research Foundation

Lundbeckfonden

Publisher

Wiley

Subject

Clinical Neurology,Neurology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ane.12885/fullpdf

Reference36 articles.

1. Rhabdomyolysis: advances in diagnosis and treatment;Parekh;Emerg Med Pract,2012