Cite

Both Heterozygous and Homozygous Loss‐of‐Function <scp> JPH3 </scp> Variants Are Associated with a Paroxysmal Movement Disorder

MLA

Dora Steel, et al. “Both Heterozygous and Homozygous Loss‐of‐Function JPH3 Variants Are Associated with a Paroxysmal Movement Disorder.” Movement Disorders, vol. 38, Oct. 2022, pp. 155–57. EBSCOhost, https://doi.org/10.1002/mds.29250.



APA

Dora Steel, Aikaterini Vezyroglou, Katy Barwick, Martin Smith, Julie Vogt, Frances M. Gibbon, J. Helen Cross, & Manju A. Kurian. (2022). Both Heterozygous and Homozygous Loss‐of‐Function JPH3 Variants Are Associated with a Paroxysmal Movement Disorder. Movement Disorders, 38, 155–157. https://doi.org/10.1002/mds.29250



Chicago

Dora Steel, Aikaterini Vezyroglou, Katy Barwick, Martin Smith, Julie Vogt, Frances M. Gibbon, J. Helen Cross, and Manju A. Kurian. 2022. “Both Heterozygous and Homozygous Loss‐of‐Function JPH3 Variants Are Associated with a Paroxysmal Movement Disorder.” Movement Disorders 38 (October): 155–57. doi:10.1002/mds.29250.