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Molecular Crosstalk Between Non-SMN-Related and SMN-Related Spinal Muscular Atrophy

Most cases of spinal muscular atrophy are caused by functional loss of the survival of motor neuron 1 ( SMN1 ) gene, while less than 5% of cases are attributed to genes other than SMN . Mutations in LMNA , the lamin A/C encoding gene, cause an adult form of spinal muscular atrophy (SMA), and in our...

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Bibliografiske detaljer
Principais autores: Darija Šoltić, Heidi R Fuller
Format: Artigo
Sprog:Inglês
Udgivet: SAGE Publishing 2020-03-01
Serier:Neuroscience Insights
Online adgang:https://doi.org/10.1177/2633105520914301
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