DCTN1 mutations in Perry syndrome.

Farrer, Matthew J

DCTN1 mutations in Perry syndrome. [electronic resource] - Nature genetics Feb 2009 - 163-5 p. digital

Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

1546-1718

10.1038/ng.293 doi


Brain--metabolism
DNA-Binding Proteins--metabolism
Depression--genetics
Dynactin Complex
Family
Female
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Hypoventilation--genetics
Male
Microtubule-Associated Proteins--genetics
Mutation--physiology
Parkinsonian Disorders--genetics
Pedigree
Syndrome
Weight Loss--genetics