When adaptive processes go awry: gain-of-function in SCN9A

Author: Young1

Source: Clinical Genetics, Volume 73, Number 1, January 2008 , pp. 34-36(3)

Publisher: Blackwell Publishing

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Abstract:

SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes

Fertleman et al. (2006)

Neuron 52: 767-774

Document Type: Research article

DOI: 10.1111/j.1399-0004.2007.00922.x

Affiliations: 1: Centre for Molecular Medicine and Therapeutics, 950 West 28th Avenue, Vancouver, BC V5Z 4H4, Canada, Email: fyoung@cmmt.ubc.ca

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