Title : A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALS.

Pub. Date : 2013 Jul

PMID : 23568759






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The dihydropyrimidinase-like 3 (DPYSL3) or Collapsin Response Mediator Protein 4a (CRMP4a) expression is modified in neurodegeneration and is involved in several ALS-associated pathways including axonal transport, glutamate excitotoxicity, and oxidative stress. Glutamic Acid dihydropyrimidinase like 3 Homo sapiens
2 The dihydropyrimidinase-like 3 (DPYSL3) or Collapsin Response Mediator Protein 4a (CRMP4a) expression is modified in neurodegeneration and is involved in several ALS-associated pathways including axonal transport, glutamate excitotoxicity, and oxidative stress. Glutamic Acid dihydropyrimidinase like 3 Homo sapiens