A LRSAM1 mutation links Charcot–Marie–Tooth type 2 to P arkinson's disease-Reference-Cited by-同舟云学术

A LRSAM1 mutation links Charcot–Marie–Tooth type 2 to P arkinson's disease

Published:2015-12-22 Issue:2 Volume:3 Page:146-149
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Aerts Marjolein B.¹,Weterman Marian A. J.²,Quadri Marialuisa³,Schelhaas H. Jurgen⁴,Bloem Bastiaan R.¹,Esselink Rianne A.¹,Baas Frank²,Bonifati Vincenzo³,Warrenburg Bart P.¹

Affiliation:

1. Department of Neurology Donders Institute for Brain, Cognition, and Behaviour Radboud University Medical Center Nijmegen The Netherlands

2. Department of Genome Analysis Academic Medical Center Amsterdam The Netherlands

3. Department of Clinical Genetics Erasmus MC Rotterdam The Netherlands

4. Epilepsy Centre Kempenhaeghe Heeze The Netherlands

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.281

Reference9 articles.

1. A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy

2. A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease

3. Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease

4. Type II Charcot‐Marie‐Tooth and dopa‐sensitive Parkinson disease;Tranchant C;Rev Neurol (Paris),1994

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