Heterozygous RAD50 gene variant in a family with systemic sclerosis suggests role of impaired DNA repair mechanisms in disease pathogenesis.

MLA

Machhua, Sanghamitra, et al. “Heterozygous RAD50 Gene Variant in a Family with Systemic Sclerosis Suggests Role of Impaired DNA Repair Mechanisms in Disease Pathogenesis.” Clinical & Experimental Dermatology, vol. 49, no. 5, May 2024, pp. 543–46. EBSCOhost, https://doi.org/10.1093/ced/llad440.

APA

Machhua, S., Sharma, S. K., Minz, R. W., Pandey, S. K., Jindal, A., Rawat, A., & Jindal, A. K. (2024). Heterozygous RAD50 gene variant in a family with systemic sclerosis suggests role of impaired DNA repair mechanisms in disease pathogenesis. Clinical & Experimental Dermatology, 49(5), 543–546. https://doi.org/10.1093/ced/llad440

Chicago

Machhua, Sanghamitra, Shefali Khanna Sharma, Ranjana Walker Minz, Saurabh Kumar Pandey, Arvind Jindal, Amit Rawat, and Ankur Kumar Jindal. 2024. “Heterozygous RAD50 Gene Variant in a Family with Systemic Sclerosis Suggests Role of Impaired DNA Repair Mechanisms in Disease Pathogenesis.” Clinical & Experimental Dermatology 49 (5): 543–46. doi:10.1093/ced/llad440.