Andreas Gal

Identification of 16 sulfamidase gene mutations including the common R74C in patients with mucopolysaccharidosis type IIIA (Sanfilippo A)

Susanna Bunge, Hüseyin İnce, Cordula Steglich et al. · Human Mutation · 1997 · 71 citations

Life Sciences, Genetics, Molecular Genetics +17

Clinical and ERG data in a family with autosomal dominant RP and Pro-347-Arg mutation in the rhodopsin gene

G�nter Niemeyer, Peter Tr�b, Albert Schinzel et al. · Documenta Ophthalmologica · 1992 · 51 citations

Life Sciences, Genetics, Molecular Genetics +8

Two different genes for X-linked retinitis pigmentosa

Brunhilde Wirth, Michael J. Denton, Jia-De Chen et al. · Genomics · 1988 · 40 citations

Medicine, Genetics, Molecular Genetics +7

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

Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneity

Andreas Gal, Brunhilde Wirth, Helena Kääriäinen et al. · Clinical Genetics · 1989 · 31 citations

Life Sciences, Genetics, Molecular Genetics +15