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- W3129761159 abstract "ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Singh S, Singh M, Dayal D, Bhatia P, Negi S, V. Attri S. Characterisation of LDL receptor gene mutations in a North Indian cohort of children with homozygous familial hypercholesterolaemia. Pediatric Endocrinology Diabetes and Metabolism. 2021;27(1):32-36. doi:10.5114/pedm.2020.103056. APA Singh, S., Singh, M., Dayal, D., Bhatia, P., Negi, S., & V. Attri, S. (2021). Characterisation of LDL receptor gene mutations in a North Indian cohort of children with homozygous familial hypercholesterolaemia. Pediatric Endocrinology Diabetes and Metabolism, 27(1), 32-36. https://doi.org/10.5114/pedm.2020.103056 Chicago Singh, Shagun, Minu Singh, Devi Dayal, Prateek Bhatia, Sandeep Negi, and Savita V. Attri. 2021. Characterisation of LDL receptor gene mutations in a North Indian cohort of children with homozygous familial hypercholesterolaemia. Pediatric Endocrinology Diabetes and Metabolism 27 (1): 32-36. doi:10.5114/pedm.2020.103056. Harvard Singh, S., Singh, M., Dayal, D., Bhatia, P., Negi, S., and V. Attri, S. (2021). Characterisation of LDL receptor gene mutations in a North Indian cohort of children with homozygous familial hypercholesterolaemia. Pediatric Endocrinology Diabetes and Metabolism, 27(1), pp.32-36. https://doi.org/10.5114/pedm.2020.103056 MLA Singh, Shagun et al. Characterisation of LDL receptor gene mutations in a North Indian cohort of children with homozygous familial hypercholesterolaemia. Pediatric Endocrinology Diabetes and Metabolism, vol. 27, no. 1, 2021, pp. 32-36. doi:10.5114/pedm.2020.103056. Vancouver Singh S, Singh M, Dayal D, Bhatia P, Negi S, V. Attri S. Characterisation of LDL receptor gene mutations in a North Indian cohort of children with homozygous familial hypercholesterolaemia. Pediatric Endocrinology Diabetes and Metabolism. 2021;27(1):32-36. doi:10.5114/pedm.2020.103056." @default.
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- W3129761159 title "Characterisation of LDL receptor gene mutations in a North Indian cohort of children with homozygous familial hypercholesterolaemia" @default.
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