Benigna von Brederlow

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

Hanno J. Bolz, Benigna von Brederlow, Alfredo Ramı́rez et al. · Nature Genetics · 2001 · 493 citations

Genetic Disorder, Genetics, Pathogenesis +6

Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p

Benigna von Brederlow, Angelika F. Hahn, Wilma J. Koopman et al. · Human Molecular Genetics · 1995 · 85 citations

Identification and in vitro expression of novelCDH23 mutations of patients with Usher syndrome type 1D

Benigna von Brederlow, Hanno J. Bolz, Andreas Janecke et al. · Human Mutation · 2002 · 45 citations

Characterization of ADAMTS14, a novel member of the ADAMTS metalloproteinase family

Hanno J. Bolz, Alfredo Ramı́rez, Benigna von Brederlow et al. · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 2001 · 31 citations

Protein Function, Natural Sciences, Genetics +5