Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination

Author:

Hu Bo1,McCollum Megan1,Ravi Vignesh1,Arpag Sezgi1,Moiseev Daniel1,Castoro Ryan2,Mobley Bret3,Burnette Bryan4,Siskind Carly5,Day John5,Yawn Robin1,Feely Shawna6,Li Yuebing7,Yan Qing18,Shy Michael6,Li Jun19ORCID

Affiliation:

1. Department of Neurology, Center for Human Genetic Research, and Vanderbilt Brain Institute; Vanderbilt University Medical Center; Nashville TN

2. Department of Physical Medicine and Rehabilitation; Vanderbilt University Medical Center; Nashville TN

3. Department of Pathology; Vanderbilt University Medical Center; Nashville TN

4. Department of Pediatrics; Vanderbilt University Medical Center; Nashville TN

5. Department of Neurology; Stanford University; Palo Alto CA

6. Department of Neurology; University of Iowa; Iowa City IA

7. Department of Neurology; Cleveland Clinic Foundation; Cleveland OH

8. Department of Laboratory Medicine; Second Affiliated Hospital of Qingdao University; Qingdao China

9. Tennessee Valley Healthcare System-Nashville VA; Nashville TN

Funder

NIH

Muscular Dystrophy Association

National Center for Advancing Translational Sciences

National Institute of Neurological Disorders and Stroke

U.S. Department of Veterans Affairs

Publisher

Wiley

Subject

Clinical Neurology,Neurology

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