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Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9 by Phatarakyijnirund, Voraluck; Mumm, Steven; McAlister, William H.; Novack, Deborah; Wenkert, Deborah; Clements, Karen L.; Whyte, Michael P. is a Medicine article available to read on EtoBox.

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Author
Phatarakyijnirund, Voraluck; Mumm, Steven; McAlister, William H.; Novack, Deborah; Wenkert, Deborah; Clements, Karen L.; Whyte, Michael P.
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 8756-3282)
Published
2016
Language
EN
Field
Medicine (Health Sciences)

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