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Article

Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice.

The Journal of neuroscience : the official journal of the Society for Neuroscience - 20 Jan 2010

Ruiz Rocío, Casañas Juan José, Torres-Benito Laura, Cano Raquel, Tabares Lucía

Abstract excerpt

Low levels of survival motor neuron (SMN) protein result in spinal muscular atrophy (SMA), a severe genetic disease characterized by motor impairment and premature lethality. Although SMN is a ubiquitous protein, motor neurons are much more vulnerable to low levels of SMN than other cells. To gai...

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Identifiers

PMID: 20089893
DOI: 10.1523/JNEUROSCI.4496-09.2010
PMCID: PMC6633088

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20089893-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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