A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci.

MLA

Baine, Fiona K., et al. “A Study of Huntington Disease-like Syndromes in Black South African Patients Reveals a Single SCA2 Mutation and a Unique Distribution of Normal Alleles across Five Repeat Loci.” Journal of the Neurological Sciences, vol. 390, July 2018, pp. 200–04. EBSCOhost, https://doi.org/10.1016/j.jns.2018.04.031.

APA

Baine, F. K., Peerbhai, N., & Krause, A. (2018). A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci. Journal of the Neurological Sciences, 390, 200–204. https://doi.org/10.1016/j.jns.2018.04.031

Chicago

Baine, Fiona K, Nabeelah Peerbhai, and Amanda Krause. 2018. “A Study of Huntington Disease-like Syndromes in Black South African Patients Reveals a Single SCA2 Mutation and a Unique Distribution of Normal Alleles across Five Repeat Loci.” Journal of the Neurological Sciences 390 (July): 200–204. doi:10.1016/j.jns.2018.04.031.