Charcot-Marie-Tooth disease type 2G redefined by a novel mutation inLRSAM1-Reference-Cited by-同舟云学术

Charcot-Marie-Tooth disease type 2G redefined by a novel mutation inLRSAM1

Published:2016-09-30 Issue:6 Volume:80 Page:823-833
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Peeters Kristien¹,Palaima Paulius¹,Pelayo-Negro Ana L.²,García Antonio³,Gallardo Elena⁴,García-Barredo Rosario⁴,Mateiu Ligia¹,Baets Jonathan¹⁵⁶,Menten Björn⁶,De Vriendt Els¹,De Jonghe Peter¹,Timmerman Vincent¹,Infante Jon²,Berciano José²,Jordanova Albena¹

Affiliation:

1. VIB Department of Molecular Genetics; University of Antwerp; Antwerp Belgium

2. Departments of Neurology; University Hospital, University of Cantabria, and Center for Biomedical Research in the Neurodegenerative Diseases Network; Santander Spain

3. Clinical Neurophysiology; University Hospital, University of Cantabria, and Center for Biomedical Research in the Neurodegenerative Diseases Network; Santander Spain

4. Radiology; University Hospital Marqués de Valdecilla (IDIVAL), University of Cantabria, and Center for Biomedical Research in the Neurodegenerative Diseases (CIBERNED) Network; Santander Spain

5. Department of Neurology; Antwerp University Hospital; Antwerp Belgium

6. Born-Bunge Institute; University of Antwerp; Antwerp Belgium

Funder

University of Antwerp

Fund for Scientific Research-Flanders

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference41 articles.

1. Genetic and clinical aspects of Charcot-Marie-Tooth's disease;Skre;Clin Genet,1974

2. Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature;Harding;J Neurol Sci,1980