Literature DB >> 9554454

Six new Gaucher disease mutations.

A Demina1, E Beutler.   

Abstract

Six previously undescribed mutations were identified in 6 unrelated Gaucher disease patients: 437C-->T (107Ser-->Leu), 593C-->T (159Pro-->Leu), 604C-->T (163Arg-->Stop), 1138G-->A (341Ala-->Thr), 1214G-->A (366Ser-->Asn), 1294T-->A (393Trp-->Arg). Five patients were compound heterozygotes and 1 patient was a 593T/593T homozygote. Four patients had type I Gaucher disease with mild clinical phenotypes. Two other patients manifested central nervous system involvement (type II and type III).

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Year:  1998        PMID: 9554454     DOI: 10.1159/000040815

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  5 in total

1.  A rare homozygous p.Arg87Trp variant of the GBA gene in Gaucher disease: A case report.

Authors:  Houweyda Jilani; Faten Hsoumi; Imen Rejeb; Yasmina Elaribi; Syrine Hizem; Molka Sebai; Arndt Rolfs; Lamia Benjemaa
Journal:  Clin Case Rep       Date:  2022-05-12

2.  First Clinicogenetic Description of Parkinson's Disease Related to GBA Mutation S107L.

Authors:  Ellen Hertz; Måns Thörnqvist; Björn Holmberg; Maciej Machaczka; Ellen Sidransky; Per Svenningsson
Journal:  Mov Disord Clin Pract       Date:  2019-03-07

3.  Novel pathogenic mutations in the glucocerebrosidase locus.

Authors:  Raquel Duran; Alisdair McNeill; Atul Mehta; Derralyn Hughes; Timothy Cox; Patrick Deegan; Anthony H V Schapira; John Hardy
Journal:  Mol Genet Metab       Date:  2012-05-18       Impact factor: 4.797

4.  Nine-year experience in Gaucher disease diagnosis at the Spanish reference center Fundación Jiménez Díaz.

Authors:  N V Ortiz-Cabrera; J Gallego-Merlo; C Vélez-Monsalve; R de Nicolas; S Fontao Mas; C Ayuso; M J Trujillo-Tiebas
Journal:  Mol Genet Metab Rep       Date:  2016-11-13

5.  Rare GBA1 genotype associated with severe bone disease in Gaucher disease type 1.

Authors:  Livia d'Avila Paskulin; Rodrigo Tzovenos Starosta; Vitória Schütt Zizemer; Suélen Basgalupp; Débora Bertholdo; Filippo Pinto E Vairo; Marina Siebert; Kristiane Michelin-Tirelli; Ida Vanessa Doederlein Schwartz
Journal:  Mol Genet Metab Rep       Date:  2019-11-22
  5 in total

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