Literature DB >> 8051940

The N370S mutation in the glucocerebrosidase gene of Portuguese type 1 Gaucher patients: linkage to the PvuII polymorphism.

L Lacerda1, O Amaral, R Pinto, J Aerts, M C Sá Miranda.   

Abstract

The mutation N370S accounts for 63% of the mutated glucocerebrosidase alleles of Portuguese type 1 Gaucher patients. It has been shown previously that this mutation is linked to the Pv1.1- form of the PvuII polymorphism and suggested that the N370S mutation in glucocerebrosidase alleles has an Ashkenazi Jewish origin. We have found that in Portuguese type 1 Gaucher patients this mutation is also invariably associated with the Pv1.1- haplotype, despite the fact that there is no evidence of Ashkenazi Jewish background in this population.

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Year:  1994        PMID: 8051940     DOI: 10.1007/bf00735401

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


  13 in total

1.  The facile detection of the nt 1226 mutation of glucocerebrosidase by 'mismatched' PCR.

Authors:  E Beutler; T Gelbart; C West
Journal:  Clin Chim Acta       Date:  1990-12-24       Impact factor: 3.786

2.  Linkage of the PvuII polymorphism with the common Jewish mutation for Gaucher disease.

Authors:  A Zimran; T Gelbart; E Beutler
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

3.  A simple salting out procedure for extracting DNA from human nucleated cells.

Authors:  S A Miller; D D Dykes; H F Polesky
Journal:  Nucleic Acids Res       Date:  1988-02-11       Impact factor: 16.971

Review 4.  Gaucher disease: new molecular approaches to diagnosis and treatment.

Authors:  E Beutler
Journal:  Science       Date:  1992-05-08       Impact factor: 47.728

5.  The human glucocerebrosidase gene and pseudogene: structure and evolution.

Authors:  M Horowitz; S Wilder; Z Horowitz; O Reiner; T Gelbart; E Beutler
Journal:  Genomics       Date:  1989-01       Impact factor: 5.736

6.  Gaucher's disease in the United Kingdom: screening non-Jewish patients for the two common mutations.

Authors:  A J Walley; M L Barth; I Ellis; A H Fensom; A Harris
Journal:  J Med Genet       Date:  1993-04       Impact factor: 6.318

7.  A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease.

Authors:  S Tsuji; P V Choudary; B M Martin; B K Stubblefield; J A Mayor; J A Barranger; E I Ginns
Journal:  N Engl J Med       Date:  1987-03-05       Impact factor: 91.245

8.  Type 1 Gaucher disease: molecular, biochemical, and clinical characterization of patients from northern Portugal.

Authors:  O Amaral; L Lacerda; R Santos; R A Pinto; H Aerts; M C Sa Miranda
Journal:  Biochem Med Metab Biol       Date:  1993-02

9.  Identification of Gaucher disease carriers: glucocerebrosidase antigen and DNA analysis.

Authors:  L Lacerda; O Amaral; R Pinto; J Aerts; M C Sá Miranda
Journal:  Biochem Med Metab Biol       Date:  1993-10

10.  Heterogeneity in type I Gaucher disease demonstrated by restriction mapping of the gene.

Authors:  J Sorge; T Gelbart; C West; B Westwood; E Beutler
Journal:  Proc Natl Acad Sci U S A       Date:  1985-08       Impact factor: 11.205

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  3 in total

1.  Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.

Authors:  G A Diaz; B D Gelb; N Risch; T G Nygaard; A Frisch; I J Cohen; C S Miranda; O Amaral; I Maire; L Poenaru; C Caillaud; M Weizberg; P Mistry; R J Desnick
Journal:  Am J Hum Genet       Date:  2000-04-21       Impact factor: 11.025

2.  Early manifestations of type 1 Gaucher disease in presymptomatic children diagnosed after parental carrier screening.

Authors:  Amy C Yang; Louise Bier; Jessica R Overbey; Jessica Cohen-Pfeffer; Khyati Desai; Robert J Desnick; Manisha Balwani
Journal:  Genet Med       Date:  2016-10-13       Impact factor: 8.822

3.  The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients.

Authors:  Jérôme Stirnemann; Marie Vigan; Dalil Hamroun; Djazia Heraoui; Linda Rossi-Semerano; Marc G Berger; Christian Rose; Fabrice Camou; Christine de Roux-Serratrice; Bernard Grosbois; Pierre Kaminsky; Alain Robert; Catherine Caillaud; Roselyne Froissart; Thierry Levade; Agathe Masseau; Cyril Mignot; Frédéric Sedel; Dries Dobbelaere; Marie T Vanier; Vassili Valayanopoulos; Olivier Fain; Bruno Fantin; Thierry Billette de Villemeur; France Mentré; Nadia Belmatoug
Journal:  Orphanet J Rare Dis       Date:  2012-10-09       Impact factor: 4.123

  3 in total

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