Steven M. Leber

Periaxin Mutations Cause Recessive Dejerine-Sottas Neuropathy

Cornelius F. Boerkoel, Hiroshi Takashima, Paweł Stankiewicz et al. · The American Journal of Human Genetics · 2001 · 216 citations · Full text

Neurodegenerative Diseases, Neurological Disorder, Degenerative Disease +5

King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene

James J. Dowling, Suzanne Lillis, Kimberley Amburgey et al. · Neuromuscular Disorders · 2011 · 111 citations

Genetics, King–denborough Syndrome, Mendelian Disorder +1

Disseminated Vaccine Strain Varicella as the Acquired Immunodeficiency Syndrome-Defining Illness in a Previously Undiagnosed Child

M. Kramer, Philip LaRussa, Wan C. Tsai et al. · PEDIATRICS · 2001 · 83 citations

Leigh Syndrome in a Girl With a Novel DLD Mutation Causing E3 Deficiency

Shane C. Quinonez, Steven M. Leber, Donna M. Martin et al. · Pediatric Neurology · 2013 · 44 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +5

The paths and destinations of the induced ipsilateral retinal projection in goldfish

Stephen S. Easter, John T. Schmidt, Steven M. Leber · Development · 1978 · 34 citations