Patricia L. Kramer

A new locus for autosomal dominant congenital cataracts maps to chromosome 3.

P. Kramer, R. Weleber, A. Billingslea, 2000, Investigative ophthalmology & visual science.

Myoclonus dystonia

L. Ozelius, R. Kurlan, R. Saunders-Pullman, 2002, Neurology.

Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family

C. Klein, P. Kramer, L. Ozelius, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Etiology of musician’s dystonia

A Münchau, E Altenmüller, E. Altenmüller, 2009, Neurology.

Adult onset idiopathic torsion dystonia is excluded from the DYT 1 region (9q34) in a Swedish family.

L Forsgren, S Fahn, X. Breakefield, 1995, Journal of neurology, neurosurgery, and psychiatry.

The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q

X. Breakefield, S. Fahn, L. Forsgren, 1994, Clinical genetics.

Rapid‐onset dystonia‐parkinsonism

X. Breakefield, E. Kasarskis, T. R. Perry, 1993, Neurology.

The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family.

N. Risch, M. Brin, J. Penney, 1998, Advances in neurology.