McDonnell, A., & Vollert, J. (2016). Inherited erythromelalgia due to mutations in SCN9A: Natural history, clinical phenotype and somatosensory profile. Brain, 139(4), . https://doi.org/10.1093/brain/aww007
Chicago Style (17th ed.) CitationMcDonnell, Aoibhinn, and Jan Vollert. "Inherited Erythromelalgia Due to Mutations in SCN9A: Natural History, Clinical Phenotype and Somatosensory Profile." Brain 139, no. 4 (2016). https://doi.org/10.1093/brain/aww007.
MLA (9th ed.) CitationMcDonnell, Aoibhinn, and Jan Vollert. "Inherited Erythromelalgia Due to Mutations in SCN9A: Natural History, Clinical Phenotype and Somatosensory Profile." Brain, vol. 139, no. 4, 2016, https://doi.org/10.1093/brain/aww007.
Warning: These citations may not always be 100% accurate.