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Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.
Defining the phenotypical spectrum associated with variants in TUBB2A.
Roles of circadian rhythmicity and sleep in human glucose regulation.
Nonimmune hydrops fetalis: a multidisciplinary approach.
Association of Vitamin D Deficiency and Treatment with COVID-19 Incidence.
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Association of Vitamin D Deficiency and Treatment with COVID-19 Incidence.
Association of Vitamin D Deficiency and Treatment with COVID-19 Incidence. medRxiv. 2020 May 13.
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authors with profiles
Vineet Arora
David Meltzer
Julian Solway
Tamara Vokes