Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking-Reference-Cited by-同舟云学术

Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking

Published:2005-12-01 Issue:2 Volume:15 Page:233-250
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Hadano Shinji,Benn Susanna C.,Kakuta Shigeru,Otomo Asako,Sudo Katsuko,Kunita Ryota,Suzuki-Utsunomiya Kyoko,Mizumura Hikaru,Shefner Jeremy M.,Cox Gregory A.,Iwakura Yoichiro,Brown Robert H.,Ikeda Joh-E

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/15/2/233/17242584/ddi440.pdf

Reference56 articles.

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4. Lerman-Sagie, T., Filiano, J., Smith, D.W. and Korson, M. (1996) Infantile onset of hereditary ascending spastic paralysis with bulbar involvement. J. Child Neurol., 11, 54–57.

5. Eymard-Pierre, E., Lesca, G., Dollet, S., Santorelli, F.M., di Capua, M., Bertini, E. and Boespflug-Tanguy, O. (2002) Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene. Am. J. Hum. Genet., 71, 518–527.

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