Literature DB >> 4758879

Sandhoff disease: diagnosis of heterozygous carriers by serum hexosaminidase assay.

Y Suzuki, Y Koizumi, H Togari, Y Ogawa.   

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Year:  1973        PMID： 4758879     DOI： 10.1016/0009-8981(73)90360-4

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


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  5 in total

Review 1.  Biochemistry and genetics of gangliosidoses.

Authors:  K Sandhoff; H Christomanou
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. I. Statistical methods.

Authors:  R M Cantor; J S Lim; C Roy; M M Kaback
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

3.  Apparent hexosaminidase B deficiency in two healthy members of a pedigree.

Authors:  P Hechtman; A Rowlands
Journal:  Am J Hum Genet       Date:  1979-07       Impact factor: 11.025

4.  Segregation of Tay-Sachs and Sandhoff alleles in a non-Jewish family.

Authors:  A B Lane; E Young; T Jenkins
Journal:  Am J Hum Genet       Date:  1980-11       Impact factor: 11.025

5.  Carrier detection in Sandhoff disease.

Authors:  J A Lowden; E J Ives; D L Keene; A L Burton; M A Skomorowski; F Howard
Journal:  Am J Hum Genet       Date:  1978-01       Impact factor: 11.025
  5 in total

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