Molecular consequences of the pathogenic mutation in feline G(M1) gangliosidosis

G(M1) gangliosidosis is an inherited, fatal neurodegenerative disease caused by deficiency of lysosomal β-D-galactosidase (EC 3.2.1.23) and consequent storage of undegraded G(M1) ganglioside. To characterize the genetic mutation responsible for feline G(M1) gangliosidosis, the normal sequence of fel...

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Main Authors: Martin, Douglas R., Rigat, Brigitte A., Foureman, Polly, Varadarajan, G.S., Hwang, Misako, Krum, Barbara K., Smith, Bruce F., Callahan, John W., Mahuran, Don J., Baker, Henry J.
Formato: Artigo
Idioma:Inglês
Publicado: 2008
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2910747/
https://ncbi.nlm.nih.gov/pubmed/18353697
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2008.02.004
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