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Article

Temporal requirement for SMN in motoneuron development.

Human molecular genetics - 1 Jul 2013

Hao Le T, Duy Phan Q, Jontes James D, Wolman Marc, Granato Michael, Beattie Christine E

Abstract excerpt

Proper function of the motor unit is dependent upon the correct development of dendrites and axons. The infant/childhood onset motoneuron disease spinal muscular atrophy (SMA), caused by low levels of the survival motor neuron (SMN) protein, is characterized by muscle denervation and paralysis. A...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 23459934
DOI: 10.1093/hmg/ddt110
PMCID: PMC3674802

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23459934-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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