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APA Citation
Abid, A., Raza, A., Khan, A. R., Firasat, S., Shahid, S., Hashmi, S., Zafar, M. N., Sultan, S., Khaliq, S., & Rizvi, S. A. (2023). primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants. Clinical genetics, 103(1), 53–66. http://access.bl.uk/ark:/81055/vdc_100172220160.0x000061