Literature DB >> 8566944

Arylsulfatase A pseudodeficiency in Chinese.

W L Hwu1, L P Tsai, W C Wang, S C Chuang, P J Wang, T R Wang.   

Abstract

Arylsulfatase A (ASA) pseudodeficiency was found to be much rarer in Taiwan than in most western countries (2.5% versus 7.3%-20% carrier rate). The linkage of two mutations (A2725G and A1788G) in the pseudodeficiency allele was preserved in Chinese, and A2725G did not occur alone. This unusual linkage of mutations has not been fully explained previously because the frequency of A2725G alone was not clear (as low as 4% in the only report). However, A1788G was found in 55 of 160 (34.4%) DNA samples tested in this study. These data suggest that the A2725G mutation occurred in DNA that already contained the A1788G change, at an ancient time in one of our common ancestors.

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Year:  1996        PMID: 8566944     DOI: 10.1007/bf02265256

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  7 in total

1.  Letter: Absence of ASA activity in healthy father of a patient with metachromatic leukodystrophy.

Authors:  G Dubois; J C Turpin; N Baumann
Journal:  N Engl J Med       Date:  1975-08-07       Impact factor: 91.245

2.  Population frequency of the arylsulphatase A pseudo-deficiency allele.

Authors:  P V Nelson; W F Carey; C P Morris
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

3.  Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site.

Authors:  V Gieselmann; A Polten; J Kreysing; K von Figura
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

4.  An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromatic leukodystrophy.

Authors:  V Gieselmann
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132

5.  Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications.

Authors:  C Hohenschutz; P Eich; W Friedl; A Waheed; E Conzelmann; P Propping
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

6.  Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease.

Authors:  J M Penzien; J Kappler; N Herschkowitz; B Schuknecht; P Leinekugel; P Propping; T Tønnesen; H Lou; H Moser; S Zierz
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

7.  Frequency of the arylsulphatase A pseudodeficiency allele in the Spanish population.

Authors:  A Chabás; S Castellvi; M Bayés; S Balcells; D Grinberg; L Vilageliu; G Marfany; W Lissens; R Gonzàlez-Duarte
Journal:  Clin Genet       Date:  1993-12       Impact factor: 4.438

  7 in total
  1 in total

1.  Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population.

Authors:  Nizar Ben Halim; Imen Dorboz; Rym Kefi; Najla Kharrat; Eleonore Eymard-Pierre; Majdi Nagara; Lilia Romdhane; Nissaf Ben Alaya-Bouafif; Ahmed Rebai; Najoua Miladi; Odile Boespflug-Tanguy; Sonia Abdelhak
Journal:  Neurol Sci       Date:  2015-11-14       Impact factor: 3.307

  1 in total

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