Mari Wold Henriksen, Kirstine Ravn, Benedicte Paus, Stephen von Tetzchner, & Ola H Skjeldal. (2018). De novo mutations in SCN1A are associated with classic Rett syndrome: A case report. BMC.
Chicago Style (17th ed.) CitationMari Wold Henriksen, Kirstine Ravn, Benedicte Paus, Stephen von Tetzchner, and Ola H Skjeldal. De Novo Mutations in SCN1A Are Associated with Classic Rett Syndrome: A Case Report. BMC, 2018.
MLA (9th ed.) CitationMari Wold Henriksen, et al. De Novo Mutations in SCN1A Are Associated with Classic Rett Syndrome: A Case Report. BMC, 2018.
Warning: These citations may not always be 100% accurate.