| Predicate | Object |
|---|---|
| rdf:type | |
| entrezgene:geneRifText |
We identified a homozygous missense mutation (c.1940 T-->C [p.647 Phe-->Ser]) of the Pleckstrin homology domain-containing, family G member 5 gene, PLEKHG5, in families with lower motor neuron disease.
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