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A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Ca(v)3.2 T-type channel activity
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the progressive loss of cortical, brain stem and spinal motor neurons that leads to muscle weakness and death. A previous study implicated CACNA1H encoding for Ca(v)3.2 calcium channels as a susceptibility gene in A...
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| Udgivet i: | Mol Brain |
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| Main Authors: | , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7060640/ https://ncbi.nlm.nih.gov/pubmed/32143681 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-020-00577-6 |
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