Launce Gouw

Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p

Launce Gouw, Craig D. Kaplan, John H. Haines et al. · Nature Genetics · 1995 · 150 citations

Molecular Neuroscience, Retina, Ophthalmology +9

Autosomal dominant cerebellar ataxia with retinal degeneration

Launce Gouw, Kathleen B. Digre, Cheryl P. Harris et al. · Neurology · 1994 · 131 citations

Genetics, Disease Gene Identification, Genetic Analysis +16

Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis

Louis J. Ptacek, Launce Gouw, Hubert Kwieciński et al. · Annals of Neurology · 1993 · 131 citations

Channelopathies, Sodium Channel Structure, Molecular Physiology +14

Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission

Launce Gouw · Human Molecular Genetics · 1998 · 102 citations · Full text

Repeat Lengths, Genetics, Genomic Mechanism +19

Proteolytic Cleavage of Ataxin-7 by Caspase-7 Modulates Cellular Toxicity and Transcriptional Dysregulation

Jessica E. Young, Launce Gouw, Stephanie Propp et al. · Journal of Biological Chemistry · 2007 · 89 citations · Full text

Retinal Neurons, Ataxin-7 Protein, Sca7 Disease Pathogenesis +19