Functional confirmation that the R1488* variant in SCN9A...

Functional confirmation that the R1488* variant in SCN9A results in complete loss-of-function of Nav1.7

He, Wen, Young, Gareth T., Zhang, Baohong, Cox, Peter J., Cho, Lily Ting-Yin, John, Sally, Paciga, Sara A., Wood, Linda S., Danziger, Nicolas, Scollen, Serena, Vangjeli, Ciara
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Volume:
19
Language:
english
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-018-0643-4
Date:
December, 2018
File:
PDF, 887 KB
english, 2018
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