Paroxysmal extreme pain disorder in family with c.3892G > T (p.Val1298Phe) in the SCN9A gene mutation – case report

Overview of attention for article published in BMC Neurology, May 2020

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ERYTHROMELALGIA RELATED RESEARCH 🔥 Paroxysmal extreme pain disorder in family with c.3892G > T (p.Val1298Phe) in the SCN9A…

ERYTHROMELALGIA RESEARCH 🔥 Paroxysmal extreme pain disorder in family with c.3892G > T (p.Val1298Phe) in the SCN9A gene…

ERYTHROMELALGIA RESEARCH JUST PUBLISHED! 🔥 Paroxysmal extreme pain disorder in family with c.3892G > T (p.Val1298Phe) in the…

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