Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities-Reference-Cited by-同舟云学术

Als2-deficient mice exhibit disturbances in endosome trafficking associated with motor behavioral abnormalities

Published:2006-06-12 Issue:25 Volume:103 Page:9595-9600
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Devon R. S.,Orban P. C.,Gerrow K.,Barbieri M. A.,Schwab C.,Cao L. P.,Helm J. R.,Bissada N.,Cruz-Aguado R.,Davidson T.-L.,Witmer J.,Metzler M.,Lam C. K.,Tetzlaff W.,Simpson E. M.,McCaffery J. M.,El-Husseini A. E.,Leavitt B. R.,Hayden M. R.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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2. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

3. AnALS2gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

4. Infantile-Onset Ascending Hereditary Spastic Paralysis Is Associated with Mutations in the Alsin Gene

5. The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings

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