bibliographic entry 2123855 [be/2123855]
https://w3id.org/oc/corpus/be/2123855
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Fertleman CR, Baker MD, Parker KA, Moffatt S, Elmslie FV, Abrahamsen B, et al (2006) SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes. Neuron 52: 767â774. PMID: 17145499
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