S. Nelson

A locus for the nystagmus-associated form of episodic ataxia maps to an 11-cM region on chromosome 19p.

J. Nutt, R. Baloh, P. Kramer, 1995, American journal of human genetics.

Hereditary endotheliopathy with retinopathy, nephropathy, and stroke(HERNS)

S. Nelson, R. Baloh, H. Vinters, 1997, Neurology.

De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy

S. Nelson, J. Graham, J. Martinez-Agosto, 2018, Genetics in Medicine.

A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia

J. Nutt, R. Baloh, J. Nutt, 1999, Neurology.

Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25

C. Sabatti, R. Baloh, T. Bosley, 2002, Neurology.