Cite
HARVARD Citation
Abid, A. et al. (2023). Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants. Clinical genetics. 103 (1), pp. 53-66. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Abid, A. et al. (2023). Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants. Clinical genetics. 103 (1), pp. 53-66. [Online].