PubMed: A Compound Heterozygous Mutation in Calpain 1 Identifies a New Genetic Cause for Spinal Muscular Atrophy Type 4 (SMA4) https://t.co/wl0xPAQqP4
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RT @gon_perez_siles: At the @KennersonLab we have shown calpain-1 is a new gene responsible for adult onset #spinalmuscularatrophy (#SMA ty…
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At the @KennersonLab we have shown calpain-1 is a new gene responsible for adult onset #spinalmuscularatrophy (#SMA type 4). Our work published in #FrontiersIn Genetics expands the number of neurodegenerative diseases caused by mutations in calpain genes.
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New Research: A Compound Heterozygous Mutation in Calpain 1 Identifies a New Genetic Cause for Spinal Muscular Atrophy Type 4 (SMA4): Spinal Muscular Atrophy (SMA) is a heterogeneous group of neuromuscular diseases characterized by degeneration… https://t.