Neutral lipid-storage disease with myopathy and Jordan anomaly

Journal article

Open access

Peer reviewed

Riccardo Zuccarino, Daniel M Anderson, Carol Holman, Shawna Feely, Laurie Gutmann and Ludwig Gutmann

Neurology, Vol.95(13), pp.599-600

09/29/2020

DOI: 10.1212/WNL.0000000000010585

PMID: 32759194

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url

https://doi.org/10.1212/WNL.0000000000010585View

Published (Version of record) Open Access

no abstract

Humans

Lipase - genetics

Lipid Metabolism, Inborn Errors - blood

Lipid Metabolism, Inborn Errors - genetics

Male

Middle Aged

Multienzyme Complexes - genetics

Muscular Diseases - blood

Muscular Diseases - genetics

Triglycerides - blood

Vacuoles - metabolism

Title: Subtitle: Neutral lipid-storage disease with myopathy and Jordan anomaly
Creators: Riccardo Zuccarino - University of Iowa Hospitals and Clinics
Daniel M Anderson - University of Iowa Hospitals and Clinics
Carol Holman - University of Iowa Hospitals and Clinics
Shawna Feely - University of Iowa Hospitals and Clinics
Laurie Gutmann - University of Iowa Hospitals and Clinics
Ludwig Gutmann - University of Iowa Hospitals and Clinics
Resource Type: Journal article
Publication Details: Neurology, Vol.95(13), pp.599-600
DOI: 10.1212/WNL.0000000000010585
PMID: 32759194
ISSN: 0028-3878
eISSN: 1526-632X
Language: English
Date published: 09/29/2020
Academic Unit: Neurology; Pathology
Record Identifier: 9984186527602771

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