Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.

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Bibliographic Details
Title: Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.
Authors: Züchner S; Center for Human Genetics, Duke University Medical Center, Durham, NC 27710, USA. szuchner@chg.duhs.duke.edu, Wang G, Tran-Viet KN, Nance MA, Gaskell PC, Vance JM, Ashley-Koch AE, Pericak-Vance MA
Source: American journal of human genetics [Am J Hum Genet] 2006 Aug; Vol. 79 (2), pp. 365-9. Date of Electronic Publication: 2006 May 26.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:0002-9297
DOI:10.1086/505361