Further evidence for specific IFIH1 mutation as a cause of Singleton-Merten syndrome with phenotypic heterogeneity.

MLA

Pettersson, Maria, et al. “Further Evidence for Specific IFIH1 Mutation as a Cause of Singleton-Merten Syndrome with Phenotypic Heterogeneity.” American Journal of Medical Genetics. Part A, vol. 173, no. 5, May 2017, pp. 1396–99. EBSCOhost, https://doi.org/10.1002/ajmg.a.38214.

APA

Pettersson, M., Bergendal, B., Norderyd, J., Nilsson, D., Anderlid, B., Nordgren, A., & Lindstrand, A. (2017). Further evidence for specific IFIH1 mutation as a cause of Singleton-Merten syndrome with phenotypic heterogeneity. American Journal of Medical Genetics. Part A, 173(5), 1396–1399. https://doi.org/10.1002/ajmg.a.38214

Chicago

Pettersson, Maria, Birgitta Bergendal, Johanna Norderyd, Daniel Nilsson, Britt‐Marie Anderlid, Ann Nordgren, and Anna Lindstrand. 2017. “Further Evidence for Specific IFIH1 Mutation as a Cause of Singleton-Merten Syndrome with Phenotypic Heterogeneity.” American Journal of Medical Genetics. Part A 173 (5): 1396–99. doi:10.1002/ajmg.a.38214.