human | Q5 |
P496 | ORCID iD | 0000-0003-4657-6454 |
P108 | employer | University of Utah | Q168515 |
Baylor College of Medicine | Q2892284 | ||
St. Joseph's Regional Medical Center | Q7589214 | ||
P735 | given name | Brian | Q15930574 |
Brian | Q15930574 | ||
P106 | occupation | researcher | Q1650915 |
Q92216810 | Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short-chain enoyl-CoA hydratase deficiency |
Q98952885 | Characterization of the Robinow syndrome skeletal phenotype, bone micro-architecture, and genotype-phenotype correlations with the osteosclerotic form |
Q90377181 | Characterization of the renal phenotype in RMND1-related mitochondrial disease |
Q90103779 | Loss of CLTRN function produces a neuropsychiatric disorder and a biochemical phenotype that mimics Hartnup disease |
Search more.