B. A. Rabin

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4).

John W Griffin, Imke Puls, K. Fischbeck, 2004, American journal of human genetics.

The sevenless + protein is expressed apically in cell membranes of developing Drosophila retina; it is not restricted to cell R7

S. Benzer, U. Banerjee, D. Hinton, 1987, Cell.

Accumulation of the adenosine triphosphate synthase subunit C in the mnd mutant mouse. A model for neuronal ceroid lipofuscinosis.

D. Price, C. Pardo, B. Rabin, 1994, The American journal of pathology.

Identification and characterization of a mouse homologue of the spinal muscular atrophy-determining gene, survival motor neuron.

D. Price, A. Bergin, S. Sisodia, 1997, Gene.

Autosomal dominant juvenile amyotrophic lateral sclerosis.

B. Crain, M. Scavina, J. Griffin, 1999, Brain : a journal of neurology.

Mapping of the kinesin-related gene ATSV to chromosome 2q37

P. Chance, M. Keller, B. Rabin, 1999, Human Genetics.

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

M. Scavina, P. Chance, J. Griffin, 1998, American journal of human genetics.