<scp>TRPV4</scp> mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of function-Reference-Cited by-同舟云学术

TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of function

Published:2022-02-16 Issue:3 Volume:9 Page:375-391
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Taga Arens¹,Peyton Margo A.¹,Goretzki Benedikt²³,Gallagher Thomas Q.⁴,Ritter Ann⁵,Harper Amy⁶,Crawford Thomas O.¹,Hellmich Ute A.²³,Sumner Charlotte J.¹⁷,McCray Brett A.¹^ORCID

Affiliation:

1. Department of Neurology Johns Hopkins University School of Medicine Baltimore Maryland 21205 USA

2. Institute of Organic Chemistry and Macromolecular Chemistry Friedrich Schiller University Jena Jena 07743 Germany

3. Centre for Biomolecular Magnetic Resonance Goethe‐University Frankfurt 60438 Germany

4. Departments of Otolaryngology – Head & Neck Surgery & Pediatrics, Eastern Virginia Medical School, and Department of Pediatric Otolaryngology Children's Hospital of the King's Daughters Norfolk Virginia 23508 USA

5. Department of Neurosurgery Virginia Commonwealth University Health System Richmond Virginia 23298 USA

6. Department of Neurology Virginia Commonwealth University Health System Richmond Virginia 23298 USA

7. The Solomon H. Snyder Department of Neuroscience Johns Hopkins University School of Medicine Baltimore Maryland 21205 USA

Funder

American Academy of Neurology

Deutsche Forschungsgemeinschaft

Muscular Dystrophy Association

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience