Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function.

MLA

Sheffer, Ruth, et al. “Postnatal Microcephaly and Pain Insensitivity Due to a de Novo Heterozygous DNM1L Mutation Causing Impaired Mitochondrial Fission and Function.” American Journal of Medical Genetics. Part A, vol. 170, no. 6, June 2016, pp. 1603–07. EBSCOhost, https://doi.org/10.1002/ajmg.a.37624.

APA

Sheffer, R., Douiev, L., Edvardson, S., Shaag, A., Tamimi, K., Soiferman, D., Meiner, V., & Saada, A. (2016). Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function. American Journal of Medical Genetics. Part A, 170(6), 1603–1607. https://doi.org/10.1002/ajmg.a.37624

Chicago

Sheffer, Ruth, Liza Douiev, Simon Edvardson, Avraham Shaag, Khaled Tamimi, Devorah Soiferman, Vardiella Meiner, and Ann Saada. 2016. “Postnatal Microcephaly and Pain Insensitivity Due to a de Novo Heterozygous DNM1L Mutation Causing Impaired Mitochondrial Fission and Function.” American Journal of Medical Genetics. Part A 170 (6): 1603–7. doi:10.1002/ajmg.a.37624.