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Aspirin Resistant Autosomal Dominant Familial Erythermalgia: A Congenital Incurable Neuropathic Disorder Caused by a Gain of Function Mutation in Exon 26 of the SCN9a Gene on Chromosome 2q24.3 | Abstract
ISSN: 2329-8790

Journal of Hematology & Thromboembolic Diseases
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Aspirin Resistant Autosomal Dominant Familial Erythermalgia: A Congenital Incurable Neuropathic Disorder Caused by a Gain of Function Mutation in Exon 26 of the SCN9a Gene on Chromosome 2q24.3

Jan Jacques Michiels*
Goodheart Institute & Foundation in Nature Medicine & Health, Rotterdam, Erasmus Free European University, Netherlands
Corresponding Author : Jan Jacques Michiels
Goodheart Institute & Foundation in Nature Medicine & Health
Rotterdam, Erasmus Free European University
Netherlands
Tel: +316-26970534
E-mail: [email protected]
Received June 12, 2014; Accepted June 13, 2014; Published June 18, 2014
Citation: Michiels JJ (2014) Aspirin Resistant Autosomal Dominant Familial Erythermalgia: A Congenital Incurable Neuropathic Disorder Caused by a Gain of Function Mutation in Exon 26 of the SCN9a Gene on Chromosome 2q24.3. J Hematol Thrombo Dis 2:e113. doi: 10.4172/2329-8790.1000e113
Copyright: © 2014, Michiels JJ. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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