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Publication | Open Access

Association of Variants in the <i>SPTLC1</i> Gene With Juvenile Amyotrophic Lateral Sclerosis

DOIFull Paper Access

78

Citations

23

References

2021

Year

Janel O. Johnson, Ruth Chia, Danny E. Miller, Rachel Li, Ravindran Kumaran, Yevgeniya Abramzon, Nada F. Alahmady, Alan E. Renton, Simon Topp, J. Raphael Gibbs,
JAMA Neurology

Abstract

These data broaden the phenotype associated with SPTLC1 and suggest that patients presenting with juvenile ALS should be screened for variants in this gene.

References

YearCitations

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