Case Report: Reinterpretation and Reclassification of ARSB:p.Arg159Cys Variant Identified in an Emirati Patient With Hearing Loss Caused by a Pathogenic Variant in the CDH23 Gene

MLA

Nahid Al Dhahouri, et al. “Case Report: Reinterpretation and Reclassification of ARSB:P.Arg159Cys Variant Identified in an Emirati Patient With Hearing Loss Caused by a Pathogenic Variant in the CDH23 Gene.” Frontiers in Pediatrics, vol. 9, Feb. 2022. EBSCOhost, https://doi.org/10.3389/fped.2021.803732.

APA

Nahid Al Dhahouri, Amanat Ali, Jozef Hertecant, & Fatma Al-Jasmi. (2022). Case Report: Reinterpretation and Reclassification of ARSB:p.Arg159Cys Variant Identified in an Emirati Patient With Hearing Loss Caused by a Pathogenic Variant in the CDH23 Gene. Frontiers in Pediatrics, 9. https://doi.org/10.3389/fped.2021.803732

Chicago

Nahid Al Dhahouri, Amanat Ali, Jozef Hertecant, and Fatma Al-Jasmi. 2022. “Case Report: Reinterpretation and Reclassification of ARSB:P.Arg159Cys Variant Identified in an Emirati Patient With Hearing Loss Caused by a Pathogenic Variant in the CDH23 Gene.” Frontiers in Pediatrics 9 (February). doi:10.3389/fped.2021.803732.