Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly.

MLA

Kar, Anjana, et al. “Whole Exome Sequencing Reveals a Mutation in ARMC9 as a Cause of Mental Retardation, Ptosis, and Polydactyly.” American Journal of Medical Genetics. Part A, vol. 176, no. 1, Jan. 2018, pp. 34–40. EBSCOhost, https://doi.org/10.1002/ajmg.a.38537.

APA

Kar, A., Phadke, S. R., Das Bhowmik, A., & Dalal, A. (2018). Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly. American Journal of Medical Genetics. Part A, 176(1), 34–40. https://doi.org/10.1002/ajmg.a.38537

Chicago

Kar, Anjana, Shubha R. Phadke, Aneek Das Bhowmik, and Ashwin Dalal. 2018. “Whole Exome Sequencing Reveals a Mutation in ARMC9 as a Cause of Mental Retardation, Ptosis, and Polydactyly.” American Journal of Medical Genetics. Part A 176 (1): 34–40. doi:10.1002/ajmg.a.38537.