Cornelis H. Schröder

Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome

Toshio Mochizuki, Henny H. Lemmink, Mariko Mariyama et al. · Nature Genetics · 1994 · 510 citations

Mendelian Disorder, Genetic Disorder, Genetics +5

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

Frank T.L. Van Der Loop, Laurence Heidet, Erika Timmer et al. · Kidney International · 2000 · 163 citations

Developmental Anomaly, Mendelian Disorder, Genetic Disorder +5

Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin

Frank T.L. Van Der Loop, L.A.H. Monnens, Cornelis H. Schröder et al. · Kidney International · 1999 · 74 citations · Full text

Autoimmune Disease, Histopathology, Pathology +7