Emerging role for sphingolipids in the genetics of amyotrophic lateral sclerosis
- PMID: 38041659
- DOI: 10.1136/jnnp-2023-332719
Emerging role for sphingolipids in the genetics of amyotrophic lateral sclerosis
Keywords: ALS; MOTOR NEURON DISEASE; NEUROGENETICS; NEUROMUSCULAR.
Conflict of interest statement
Competing interests: None declared.
Comment on
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Recurrent de novo SPTLC2 variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis.J Neurol Neurosurg Psychiatry. 2024 Jan 11;95(2):103-113. doi: 10.1136/jnnp-2023-332132. J Neurol Neurosurg Psychiatry. 2024. PMID: 38041679 Free PMC article.
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