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1. Case–Control and Family‐Based Association Study of Specific PTPRD Variants in Restless Legs Syndrome. Issue 5 (9th January 2016)

2. CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders. (June 2017)

3. Differential expression of microRNAs associated with neurodegenerative diseases and diabetic nephropathy in protein l‐isoaspartyl methyltransferase‐deficient mice. (5th August 2021)

4. Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder. Issue 6 (14th May 2018)

5. Genetic predisposition to increased serum calcium, bone mineral density, and fracture risk in individuals with normal calcium levels: mendelian randomisation study. (1st August 2019)