Gene therapy, CMT1X, and the inherited neuropathies

Letter/Communication

Open access

Michael E Shy

Proceedings of the National Academy of Sciences - PNAS, Vol.113(17), pp.4552-4554

04/26/2016

DOI: 10.1073/pnas.1604005113

PMCID: PMC4855541

PMID: 27078106

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https://doi.org/10.1073/pnas.1604005113View

Published (Version of record) Open Access

Commentary

Connexins - genetics

Genetic Therapy

Humans

Charcot-Marie-Tooth Disease - genetics

Title: Subtitle: Gene therapy, CMT1X, and the inherited neuropathies
Creators: Michael E Shy - Department of Neurology, University of Iowa, Iowa City, IA 52242 michael-shy@uiowa.edu
Resource Type: Letter/Communication
Publication Details: Proceedings of the National Academy of Sciences - PNAS, Vol.113(17), pp.4552-4554
DOI: 10.1073/pnas.1604005113
PMID: 27078106
PMCID: PMC4855541
NLM abbreviation: Proc Natl Acad Sci U S A
ISSN: 0027-8424
eISSN: 1091-6490
Publisher: National Academy of Sciences; United States
Grant note: R01 NS075764 / NINDS NIH HHS U54 NS065712 / NINDS NIH HHS
Language: English
Date published: 04/26/2016
Academic Unit: Neurology; Molecular Physiology and Biophysics; Stead Family Department of Pediatrics; Iowa Neuroscience Institute
Record Identifier: 9984020626602771

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