Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

Published

Journal Article

Amyotrophic lateral sclerosis (ALS) usually presents as a sporadic disorder of motor neurons. However, familial forms of ALS have been described--autosomal dominant forms (ALS1, ALS3), clinically indistinguishable from the sporadic form, and autosomal recessive forms with early onset and slower progression of symptoms (ALS2). To localize the gene for one of the autosomal recessive forms of ALS, we applied linkage analysis to a large inbred family from Tunisia. A lod score maximum of Zmax = 8.2 at theta = 0.00 was obtained with marker D2S72 located on chromosome 2q33-q35. The fine mapping of this region suggested that the ALS2 locus lies in the 8 cM segment flanked by D2S155 and D2S115.

Full Text

Duke Authors

Cited Authors

  • Hentati, A; Bejaoui, K; Pericak-Vance, MA; Hentati, F; Speer, MC; Hung, WY; Figlewicz, DA; Haines, J; Rimmler, J; Ben Hamida, C

Published Date

  • July 1994

Published In

Volume / Issue

  • 7 / 3

Start / End Page

  • 425 - 428

PubMed ID

  • 7920663

Pubmed Central ID

  • 7920663

International Standard Serial Number (ISSN)

  • 1061-4036

Digital Object Identifier (DOI)

  • 10.1038/ng0794-425

Language

  • eng

Conference Location

  • United States