Molecular genetics of an autosomal dominant form of torsion dystonia.

P. L. Kramer, L. Ozelius, M. F. Brin, S. Fahn, K. K. Kidd, J. Gusella, X. O. Breakefield

Research output: Contribution to journalArticle

7 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)57-66
Number of pages10
JournalAdvances in neurology
Volume50
StatePublished - 1988
Externally publishedYes

Fingerprint

Dystonia Musculorum Deformans
Dominant Genes
Genetic Linkage
Pedigree
Genetic Markers
Chromosome Aberrations
Restriction Fragment Length Polymorphisms
Molecular Biology
DNA
Genes

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Kramer, P. L., Ozelius, L., Brin, M. F., Fahn, S., Kidd, K. K., Gusella, J., & Breakefield, X. O. (1988). Molecular genetics of an autosomal dominant form of torsion dystonia. Advances in neurology, 50, 57-66.

Molecular genetics of an autosomal dominant form of torsion dystonia. / Kramer, P. L.; Ozelius, L.; Brin, M. F.; Fahn, S.; Kidd, K. K.; Gusella, J.; Breakefield, X. O.

In: Advances in neurology, Vol. 50, 1988, p. 57-66.

Research output: Contribution to journalArticle

Kramer, PL, Ozelius, L, Brin, MF, Fahn, S, Kidd, KK, Gusella, J & Breakefield, XO 1988, 'Molecular genetics of an autosomal dominant form of torsion dystonia.', Advances in neurology, vol. 50, pp. 57-66.
Kramer PL, Ozelius L, Brin MF, Fahn S, Kidd KK, Gusella J et al. Molecular genetics of an autosomal dominant form of torsion dystonia. Advances in neurology. 1988;50:57-66.
Kramer, P. L. ; Ozelius, L. ; Brin, M. F. ; Fahn, S. ; Kidd, K. K. ; Gusella, J. ; Breakefield, X. O. / Molecular genetics of an autosomal dominant form of torsion dystonia. In: Advances in neurology. 1988 ; Vol. 50. pp. 57-66.
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