Heike Wedemann

Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa

Susanna Bunge, Heike Wedemann, D. David et al. · Genomics · 1993 · 121 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene.

E Apfelstedt-Sylla, Marc Theischen, Klaus Rüther et al. · British Journal of Ophthalmology · 1995 · 68 citations · Full text

Medicine, Genetics, Ophthalmology +17

Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD)

Sigrid Fuchs, Claude Olivier Sarde, Heike Wedemann et al. · Human Molecular Genetics · 1994 · 60 citations

Life Sciences, Genetics, Molecular Genetics +11

Missense mutation (Arg121Trp) in the norrie disease gene associated with X-linked exudative vitreoretinopathy

Sigrid Fuchs, Ulrich Kellner, Heike Wedemann et al. · Human Mutation · 1995 · 32 citations

Life Sciences, Genetics, Ophthalmology +15

A missense point mutation (Leu13Arg) of the Norrie disease gene in a large Cuban kindred with Norrie disease

Sigrid Fuchs, Shijun Xu, Manuel Caballero et al. · Human Molecular Genetics · 1994 · 20 citations

Life Sciences, Genetics, Molecular Genetics +15