Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease

Coro Paisán‐Ruíz, Shushant Jain, E. Whitney Evans et al. · Neuron · 2004 · 2.4K citations · Full text

Neurodegenerative Diseases, Genetic Disorder, Parkinson Disease +9

CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS

A. E. Harding · The Lancet · 1983 · 954 citations

Neurological Disorder, Genetic Disorder, Degenerative Disease +4

HOMOSEXUALITY AS A CRIME.

Pask Ea, Lunn Jn · PubMed · 1965 · 338 citations

Sexual Cultures, Queer Politics, A Crime +10

The K–Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum

Heidi Howard, David B. Mount, Daniel Rochefort et al. · Nature Genetics · 2002 · 277 citations

K–cl Cotransporter Kcc3, Synaptic Transmission, Corpus Callosum +17

Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia

Michael A. Simpson, Christos Proukakis, Anna Pryde et al. · The American Journal of Human Genetics · 2003 · 173 citations · Full text

Complicated Form, Mast Cell Disorder, Mast Syndrome +6