Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?

Author:

Werheid Friederike12,Azzedine Hamid2,Zwerenz Eva12,Bozkurt Ahmet34,Moeller Marcus J.5,Lin Lilian12,Mull Michael6,Häusler Martin7,Schulz Jörg B.18,Weis Joachim2,Claeys Kristl G.129

Affiliation:

1. Department of Neurology University Hospital RWTH Aachen Aachen Germany

2. Institute of Neuropathology University Hospital RWTH Aachen Aachen Germany

3. Department of Plastic and Reconstructive Surgery Hand Surgery‐Burn Center University Hospital RWTH Aachen Aachen Germany

4. Department of Plastic & Aesthetic, Reconstructive & Hand Surgery Center for Reconstructive Microsurgery and Peripheral Nerve Surgery (ZEMPEN) Agaplesion Markus Hospital Frankfurt am Main Germany

5. Section Immunology and Nephrology Department of Internal Medicine University Hospital RWTH Aachen Aachen Germany

6. Department of Neuroradiology University Hospital RWTH Aachen Aachen Germany

7. Division of Neuropediatrics and Social Pediatrics Department of Pediatrics University Hospital RWTH Aachen Aachen Germany

8. JARA – Translational Brain Medicine Aachen Germany

9. Department of Neurology University Hospitals Leuven and University of Leuven (KU Leuven) Leuven Belgium

Funder

Deutsche Gesellschaft für Muskelkranke e.V. (DGM)

Publisher

Wiley

Subject

Behavioral Neuroscience

Reference47 articles.

1. Ananth U. Athena Diagnostics Inc. 1999. Personal data.http://www.molgen.ua.ac.be/cmtmutations/Mutations/Mutations.cfm

2. Observations on hypertrophic neuropathy of Dejerine and Sottas

3. Molecular genetics of charcot‐marie‐tooth disease: from genes to genomes;Azzedine H.;Mol. Syndromol.,2012

4. Fatigue, reduced sleep quality and restless legs syndrome in Charcot-Marie-Tooth disease: a web-based survey

5. Sleep disorders in Charcot-Marie-Tooth disease type 1

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