Cita APA (7a ed.)
Wang, S., Xu, C. Y., Zhu, Y., Ding, W., Hu, J., Xu, B., . . . Liu, X. (2024). A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese family. Orphanet Journal of Rare Diseases, 19(1), 1-13.
Cita Chicago Style (17a ed.)
Wang, Suyang, Chen Yang Xu, Yiming Zhu, Wenjuan Ding, Jieyu Hu, Baicheng Xu, Yufen Guo, y Xiaowen Liu. "A Rare Transcript Homozygous Variants in CLRN1(USH3A) Causes Usher Syndrome Type 3 in a Chinese Family." Orphanet Journal of Rare Diseases 19, no. 1 (2024): 1-13.
Cita MLA (9a ed.)
Wang, Suyang, et al. "A Rare Transcript Homozygous Variants in CLRN1(USH3A) Causes Usher Syndrome Type 3 in a Chinese Family." Orphanet Journal of Rare Diseases, vol. 19, no. 1, 2024, pp. 1-13.
Precaución: Estas citas no son 100% exactas.