Skip to main content
Journal cover image

An intragenic modifier of hereditary spastic paraplegia due to spastin gene mutation suggests a role for cyclin-dependent kinase 5 in HSP pathogenesis.

Publication ,  Conference
Svenson, IK; Kloos, MT; Gaskell, PC; Nance, MA; Garbern, JY; Pericak-Vance, MA; Ashley-Koch, AE; Marchuk, DA
Published in: AMERICAN JOURNAL OF HUMAN GENETICS
November 1, 2003

Duke Scholars

Published In

AMERICAN JOURNAL OF HUMAN GENETICS

ISSN

0002-9297

Publication Date

November 1, 2003

Volume

73

Issue

5

Start / End Page

550 / 550

Location

LOS ANGELES, CALIFORNIA

Publisher

UNIV CHICAGO PRESS

Conference Name

Annual Meeting of the American-Society-of-Human-Genetics

Related Subject Headings

  • Genetics & Heredity
  • 42 Health sciences
  • 32 Biomedical and clinical sciences
  • 31 Biological sciences
  • 11 Medical and Health Sciences
  • 06 Biological Sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Svenson, I. K., Kloos, M. T., Gaskell, P. C., Nance, M. A., Garbern, J. Y., Pericak-Vance, M. A., … Marchuk, D. A. (2003). An intragenic modifier of hereditary spastic paraplegia due to spastin gene mutation suggests a role for cyclin-dependent kinase 5 in HSP pathogenesis. In AMERICAN JOURNAL OF HUMAN GENETICS (Vol. 73, pp. 550–550). LOS ANGELES, CALIFORNIA: UNIV CHICAGO PRESS.
Svenson, I. K., M. T. Kloos, P. C. Gaskell, M. A. Nance, J. Y. Garbern, M. A. Pericak-Vance, A. E. Ashley-Koch, and D. A. Marchuk. “An intragenic modifier of hereditary spastic paraplegia due to spastin gene mutation suggests a role for cyclin-dependent kinase 5 in HSP pathogenesis.” In AMERICAN JOURNAL OF HUMAN GENETICS, 73:550–550. UNIV CHICAGO PRESS, 2003.
Svenson IK, Kloos MT, Gaskell PC, Nance MA, Garbern JY, Pericak-Vance MA, et al. An intragenic modifier of hereditary spastic paraplegia due to spastin gene mutation suggests a role for cyclin-dependent kinase 5 in HSP pathogenesis. In: AMERICAN JOURNAL OF HUMAN GENETICS. UNIV CHICAGO PRESS; 2003. p. 550–550.
Svenson, I. K., et al. “An intragenic modifier of hereditary spastic paraplegia due to spastin gene mutation suggests a role for cyclin-dependent kinase 5 in HSP pathogenesis.AMERICAN JOURNAL OF HUMAN GENETICS, vol. 73, no. 5, UNIV CHICAGO PRESS, 2003, pp. 550–550.
Svenson IK, Kloos MT, Gaskell PC, Nance MA, Garbern JY, Pericak-Vance MA, Ashley-Koch AE, Marchuk DA. An intragenic modifier of hereditary spastic paraplegia due to spastin gene mutation suggests a role for cyclin-dependent kinase 5 in HSP pathogenesis. AMERICAN JOURNAL OF HUMAN GENETICS. UNIV CHICAGO PRESS; 2003. p. 550–550.
Journal cover image

Published In

AMERICAN JOURNAL OF HUMAN GENETICS

ISSN

0002-9297

Publication Date

November 1, 2003

Volume

73

Issue

5

Start / End Page

550 / 550

Location

LOS ANGELES, CALIFORNIA

Publisher

UNIV CHICAGO PRESS

Conference Name

Annual Meeting of the American-Society-of-Human-Genetics

Related Subject Headings

  • Genetics & Heredity
  • 42 Health sciences
  • 32 Biomedical and clinical sciences
  • 31 Biological sciences
  • 11 Medical and Health Sciences
  • 06 Biological Sciences