Literature DB >> 1171773

Assignment of the human gene for hexosaminidase B to chromosome 5.

H J Boedecker, W J Mellman, T A Tedesco, C M Croce.   

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Year:  1975        PMID： 1171773     DOI： 10.1016/0014-4827(75)90473-5

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN： 0014-4827            Impact factor:   3.905


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  3 in total

1.  Characterization of heteropolymeric hexosaminidase A in human X mouse hybrid cells.

Authors:  J Chern; E Beutler; W Kuhl; F Gilbert; W J Mellman; C M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  1976-10       Impact factor: 11.205

2.  Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease.

Authors:  M Cohen-Tannoudji; P Marchand; S Akli; S A Sheardown; J P Puech; C Kress; P Gressens; M C Nassogne; T Beccari; A L Muggleton-Harris
Journal:  Mamm Genome       Date:  1995-12       Impact factor: 2.957

3.  Structure and distribution of an Alu-type deletion mutation in Sandhoff disease.

Authors:  K Neote; B McInnes; D J Mahuran; R A Gravel
Journal:  J Clin Invest       Date:  1990-11       Impact factor: 14.808
  3 in total

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