Volume 44, Issue 4 pp. 499-502
Main Article

Confirmation of the severe phenotypic effect of serine at codon 41 of the superoxide dismutase 1 gene

S. H. Subramony MD

Corresponding Author

S. H. Subramony MD

Department of Neurology, University of Florida College of Medicine and McKnight Brain Institute, P.O. Box 100236, 100 South Newell Drive, Room 3-100, Gainesville, Florida 32610, USA

Department of Neurology, University of Florida College of Medicine and McKnight Brain Institute, P.O. Box 100236, 100 South Newell Drive, Room 3-100, Gainesville, Florida 32610, USASearch for more papers by this author
Tetsuo Ashizawa MD

Tetsuo Ashizawa MD

Department of Neurology, University of Florida College of Medicine and McKnight Brain Institute, P.O. Box 100236, 100 South Newell Drive, Room 3-100, Gainesville, Florida 32610, USA

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Leigh Langford MS

Leigh Langford MS

Department of Neurology, University of Mississippi Medical Center, Jackson, Mississippi, USA

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Robert Mckenna PhD

Robert Mckenna PhD

IDS Biochemistry and Molecular Biology, University of Florida, Gainesville, Florida, USA

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Balu Avvaru PhD

Balu Avvaru PhD

IDS Biochemistry and Molecular Biology, University of Florida, Gainesville, Florida, USA

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Teepu Siddique MD, PhD

Teepu Siddique MD, PhD

Davee Department of Neurology and Clinical Neurosciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA

Department of Cell and Molecular Biology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA

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V. Vedanarayanan MD

V. Vedanarayanan MD

Department of Neurology, University of Mississippi Medical Center, Jackson, Mississippi, USA

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First published: 31 March 2011
Citations: 1

Abstract

Introduction: A Gly41Ser mutation in the superoxide dismutase 1 gene (SOD1) has been reported to cause a very rapid course of amyotrophic lateral sclerosis (ALS) in a limited number of Italian patients, but a Gly41Asp mutation results in a more benign course. Methods: Four members of an African American family with autosomal dominant ALS were evaluated clinically over 12 years. Mutation analysis of SOD1 was done on 1 patient. Results: All patients had a pure lower motor neuron syndrome with onset to death in 9–15 months. A Gly41Ser mutation in SOD1 was established. In silico modeling suggested that this mutation can have a more deleterious effect than a Gly41Asp mutation. Conclusion: The more rapid course of ALS with the Gly41Ser SOD1 mutation is confirmed in a distinct ethnic group. Muscle Nerve, 2011

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