F, R., L, B., M, C., J, R., A, D., G, S., . . . ET, L. (2023). Characterization of novel CACNA1A splice variants by RNA-sequencing in patients with episodic or congenital ataxia. Clinical genetics, 104(3), 365. https://doi.org/10.1111/cge.14358
Chicago Style (17th ed.) CitationF, Riant, et al. "Characterization of Novel CACNA1A Splice Variants by RNA-sequencing in Patients with Episodic or Congenital Ataxia." Clinical Genetics 104, no. 3 (2023): 365. https://doi.org/10.1111/cge.14358.
MLA (9th ed.) CitationF, Riant, et al. "Characterization of Novel CACNA1A Splice Variants by RNA-sequencing in Patients with Episodic or Congenital Ataxia." Clinical Genetics, vol. 104, no. 3, 2023, p. 365, https://doi.org/10.1111/cge.14358.
Warning: These citations may not always be 100% accurate.