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A Rare Case of Vacuolar Myopathy (P3.120)

Year: 2017

Type: article

Study design: Case Report

Source: Neurology

DOI: 10.1212/wnl.88.16_supplement.p3.120

Authors: Robert Murphy, Mazen Dimachkie, Melanie Glenn, Omar Jawdat, Jeffrey Statland, Richard Barohn, Laura Herbelin, Mamatha Pasnoor

Institution: University of Kansas Medical Center

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2901876065

FWCI:

Cites:

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Related to: 10