Literature DB >> 8127064

Pseudodeficiency of alpha-iduronidase.

H A Taylor1, G H Thomas.   

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Year:  1993        PMID： 8127064     DOI： 10.1007/bf00711533

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


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  2 in total

Review 1.  A nonpathologic allele (IW) for low alpha-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome.

Authors:  C B Whitley; R J Gorlin; W Krivit
Journal:  Am J Med Genet       Date:  1987-09

2.  Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cells.

Authors:  R Gatti; C Borrone; M Filocamo; N Pannone; P Di Natale
Journal:  Prenat Diagn       Date:  1985 Mar-Apr       Impact factor: 3.050
  2 in total
  2 in total

Review 1.  "Pseudodeficiencies" of lysosomal hydrolases.

Authors:  G H Thomas
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

2.  Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiency.

Authors:  E L Aronovich; D Pan; C B Whitley
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025
  2 in total

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