Work

Phenotypic and muscle biopsy features of patients with FKRP c.1387A>G founder mutation (P5.454)

Year: 2018

Type: article

Study design: Case Report

Source: Neurology

DOI: 10.1212/wnl.90.15_supplement.p5.454

Authors: Angela Lee, Karra Jones, Katherine Mathews, Steven Moore, Russell Butterfield, Nicholas Johnson, Chamindra Konersman, Jose Abdenur, Brent Beson

Institutions: University of Iowa, Primary Children's Hospital, University of Utah, University of California San Diego, Children's Hospital of Orange County, INTEGRIS Baptist Medical Center, INTEGRIS Southwest 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: W4389436464

FWCI:

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