Carter, M. T., McMillan, H. J., Tomin, A., & Weiss, N. (2019). Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy. Channels (Austin).
Citação norma ChicagoCarter, Melissa T., Hugh J. McMillan, Andriy Tomin, and Norbert Weiss. "Compound Heterozygous CACNA1H Mutations Associated With Severe Congenital Amyotrophy." Channels (Austin) 2019.
Citação norma MLACarter, Melissa T., Hugh J. McMillan, Andriy Tomin, and Norbert Weiss. "Compound Heterozygous CACNA1H Mutations Associated With Severe Congenital Amyotrophy." Channels (Austin) 2019.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.