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Spontaneous appearance of Tay–Sachs disease in an animal model

  • Published:2008-09 Issue:1-2 Volume:95 Page:59-65
  • ISSN:1096-7192
  • Container-title:Molecular Genetics and Metabolism
  • language:en
  • Short-container-title:Molecular Genetics and Metabolism

Author:

Zeng B.J.,Torres P.A.,Viner T.C.,Wang Z.H.,Raghavan S.S.,Alroy J.,Pastores G.M.,Kolodny E.H.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference42 articles.

1. Molecular analysis of the HEXA gene in Italian patients with infantile and late onset Tay–Sachs disease: detection of fourteen novel alleles;Montalvo;Hum. Mutat.,2005

2. The Gm2 gangliosidoses;Gravel,2001

3. Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay–Sachs disease;Triggs-Raine;Am. J. Hum. Genet.,1991

4. Organization of the gene encoding the human B-hexosaminidase α-chain;Proia;J. Biol. Chem.,1987

5. Bone marrow transplantation prolongs life span and ameliorates neurologic manifestation in Sandhoff disease mice;Norflus;J. Clin. Invest.,1998

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