R. Bashir

Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development

Louise V.B. Anderson, Kenneth Davison, Jessica Moss et al. · Human Molecular Genetics · 1999 · 296 citations

Medicine, Genetics, Molecular Biology +15

Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s)

Tracey Weiler, R. Bashir, Louise V.B. Anderson et al. · Human Molecular Genetics · 1999 · 179 citations

Life Sciences, Genetics, Molecular Genetics +16

Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site

T J Keen, C.F. Inglehearn, Douglas H. Lester et al. · Genomics · 1991 · 169 citations

Medicine, Genetics, Ophthalmology +14

Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy

Masashi Aoki, J. Liu, Isabelle Richard et al. · Neurology · 2001 · 146 citations · Full text

Medicine, Genetics, Molecular Genetics +16

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.

C.F. Inglehearn, R. Bashir, Douglas H. Lester et al. · PubMed · 1991 · 139 citations · Full text

Medicine, Genetics, Molecular Genetics +12