about
A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagenIncidence of end-stage renal disease in the Turkish-Cypriot population of Northern Cyprus: a population based studyCombinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.Mutations in mitochondrial DNA causing tubulointerstitial kidney disease.Genetic testing can resolve diagnostic confusion in Alport syndrome.
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description
researcher ORCID ID = 0000-0002-5896-7084
@en
wetenschapper
@nl
name
Thomas M Connor
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Thomas M Connor
@en
Thomas M Connor
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Thomas M Connor
@nl
type
label
Thomas M Connor
@ast
Thomas M Connor
@en
Thomas M Connor
@es
Thomas M Connor
@nl
prefLabel
Thomas M Connor
@ast
Thomas M Connor
@en
Thomas M Connor
@es
Thomas M Connor
@nl
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0000-0002-5896-7084