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SPTLC1 Mutations Associated with Early Onset Amyotrophic Lateral Sclerosis Impair ORMDL Regulation

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Year: 2021
Type: article
Source: The FASEB Journal
DOI: 10.1096/fasebj.2021.35.s1.00013
Authors: Teresa Dunn, Kenneth Gable, Sita Gupta, Payam Mohassel, Carsten Bönnemann, Zoe Piccus, Claire Le Pichon, Richard Proia, Chia‐Hsueh Lee
Institutions: Uniformed Services University of the Health Sciences, National Institutes of Health, National Institute of Neurological Disorders and Stroke, St. Jude Children's Research Hospital
Language: English

Topic: Amyotrophic Lateral Sclerosis Research
Subfield: Neurology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: Congressionally Directed Medical Research Programs
Award: SPT-Associated ALS, a New Paradigm for Disease: Mouse and Fly Models for Identifying and Testing Therapeutic Targets
OpenAlex ID: W3162510879
FWCI:
Cites:
Cited by:
Related to: 10
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