Literature DB >> 9870214

Unusual pure motor axonal neuropathy in a Burmese family with galactosialidosis.

E K Tan1, M C Wong, I Ng, S H Teo, Y L Lo, M M Cho.   

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Year:  1998        PMID： 9870214     DOI： 10.1023/a:1005431021025

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  2 in total

1.  Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man.

Authors:  A D'Azzo; A Hoogeveen; A J Reuser; D Robinson; H Galjaard
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

2.  The chromosomal localization of human beta-galactosidase revisited: a locus for beta-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22.

Authors:  H J Sips; H A de Wit-Verbeek; J de Wit; A Westerveld; H Galjaard
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132
  2 in total

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