Novel Mutations in the DYNC1H1 Tail Domain Refine the Genetic and Clinical Spectrum of Dyneinopathies-Reference-Cited by-同舟云学术

Novel Mutations in the DYNC1H1 Tail Domain Refine the Genetic and Clinical Spectrum of Dyneinopathies

Published:2015-03 Issue:3 Volume:36 Page:287-291
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Peeters Kristien¹²,Bervoets Sven¹²,Chamova Teodora³,Litvinenko Ivan⁴,De Vriendt Els¹²,Bichev Stoyan⁵,Kancheva Dahlia¹²⁶,Mitev Vanyo⁶,Kennerson Marina⁷,Timmerman Vincent²⁸,De Jonghe Peter²⁹¹⁰,Tournev Ivailo³¹¹,MacMillan John¹²,Jordanova Albena¹²⁶

Affiliation:

1. Molecular Neurogenomics Group; Department of Molecular Genetics; VIB; Antwerp Belgium

2. Neurogenetics Laboratory; Institute Born-Bunge; University of Antwerp; Antwerp Belgium

3. Department of Neurology; Medical University-Sofia; Sofia Bulgaria

4. Clinic of Child Neurology; Department of Pediatrics; Medical University-Sofia; Sofia Bulgaria

5. Laboratory of Clinical Genetics; University Hospital “Maychin dom”; Medical University-Sofia; Sofia Bulgaria

6. Department of Medical Chemistry and Biochemistry; Molecular Medicine Center; Medical University-Sofia; Sofia Bulgaria

7. Northcott Neuroscience Laboratory; ANZAC Research Institute; Molecular Medicine Laboratory; Concord Hospital; Sydney Medical School; University of Sydney; New South Wales Australia

8. Peripheral Neuropathy Group; Department of Molecular Genetics; VIB; Antwerp Belgium

9. Neurogenetics Group; Department of Molecular Genetics; VIB; Antwerp Belgium

10. Division of Neurology; University Hospital Antwerp (UZA); Antwerp Belgium

11. Department of Cognitive Science and Psychology; New Bulgarian University; Sofia Bulgaria

12. Genetic Health Queensland; Royal Brisbane and Women's Hospital; Herston Qld Australia

Funder

Fonds Wetenschappelijk Onderzoek

National Health and Medical Research Council

Agentschap voor Innovatie door Wetenschap en Technologie

European Commission

Belgian Association against Neuromuscular Disorders

Medical Foundation Queen Elisabeth