MICHAEL BRAUN to Mutation
This is a "connection" page, showing publications MICHAEL BRAUN has written about Mutation.
Connection Strength
0.206
-
Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report. BMC Nephrol. 2017 Jul 18; 18(1):243.
Score: 0.142
-
Characterization of the renal phenotype in RMND1-related mitochondrial disease. Mol Genet Genomic Med. 2019 12; 7(12):e973.
Score: 0.041
-
Variants in genes coding for collagen type IV a-chains are frequent causes of persistent, isolated hematuria during childhood. Pediatr Nephrol. 2023 03; 38(3):687-695.
Score: 0.012
-
Natural genetic variation in Stim1 creates stroke in the spontaneously hypertensive rat. Genes Immun. 2020 05; 21(3):182-192.
Score: 0.011