Normal view MARC view ISBD view

Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations.

Pfeffer, Gerald

Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations. [electronic resource] - Neurology Dec 2013 - 2073-81 p. digital

Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Review

ISSN: 1526-632X

Standard No.: 10.1212/01.wnl.0000437308.22603.43 doi

Subjects--Topical Terms:
Adolescent
Adult
Cohort Studies
DNA, Mitochondrial--genetics
Female
Humans
Male
Multiple Sclerosis--diagnosis
Mutation--genetics
Optic Atrophy, Hereditary, Leber--diagnosis
Prospective Studies
United Kingdom--epidemiology
Young Adult

Print
Cite
Add to your cart (remove)
Save record
BIBTEX Dublin Core MARCXML MARC (non-Unicode/MARC-8) MARC (Unicode/UTF-8) MARC (Unicode/UTF-8, Standard) MODS (XML) RIS ISBD
More searches

Search for this title in:
Other Libraries (WorldCat) Other Databases (Google Scholar) Online Stores (Bookfinder.com) Open Library (openlibrary.org)