Literature DB >> 7860075

De novo missense mutation Y174S in exon 1 of the adrenoleukodystrophy (ALD) gene.

A Barceló1, M Girós, C O Sarde, G Pintos, J L Mandel, T Pàmpols, X Estivill.   

Abstract

Adrenoleukodystrophy (ALD) is an X-linked disease, characterised by an alteration of the peroxisomal beta-oxidation of the very long chain fatty acids. The ALD gene has been identified and mutations have been detected in ALD patients. We report here a new missense mutation in the ALD gene of a male patient, predicting a tyrosine to serine substitution at codon 174 (mutation Y174S). The mother of the ALD patient does not have the Y174S mutation in her leukocyte DNA, indicating that Y174S arose de novo in the patient. Y174S is the first reported de novo mutation in the ALD gene.

Entities:  

Mesh:

Year:  1995        PMID: 7860075     DOI: 10.1007/bf00209412

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


  11 in total

1.  Genetic variation of microsatellite markers D1S117, D6S89, D11S35, APOC2, and D21S168 in the Spanish population.

Authors:  J J Fuentes; I Banchs; V Volpini; X Estivill
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

2.  Identification of a new frameshift mutation (1801delAG) in the ALD gene.

Authors:  A Barceló; M Girós; C O Sarde; A Martínez-Bermejo; J L Mandel; T Pàmpols; X Estivill
Journal:  Hum Mol Genet       Date:  1994-10       Impact factor: 6.150

3.  Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophy.

Authors:  A Uchiyama; Y Suzuki; X Q Song; T Fukao; A Imamura; S Tomatsu; N Shimozawa; N Kondo; T Orii
Journal:  Biochem Biophys Res Commun       Date:  1994-01-28       Impact factor: 3.575

4.  Specific diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point-mutation (G985) in the MCAD gene.

Authors:  N Gregersen; A I Blakemore; V Winter; B Andresen; S Kølvraa; L Bolund; D Curtis; P C Engel
Journal:  Clin Chim Acta       Date:  1991-11-09       Impact factor: 3.786

5.  Identification of mutations in the putative ATP-binding domain of the adrenoleukodystrophy gene.

Authors:  P Fanen; S Guidoux; C O Sarde; J L Mandel; M Goossens; P Aubourg
Journal:  J Clin Invest       Date:  1994-08       Impact factor: 14.808

6.  Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome.

Authors:  J Gärtner; H Moser; D Valle
Journal:  Nat Genet       Date:  1992-04       Impact factor: 38.330

7.  Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters.

Authors:  J Mosser; A M Douar; C O Sarde; P Kioschis; R Feil; H Moser; A M Poustka; J L Mandel; P Aubourg
Journal:  Nature       Date:  1993-02-25       Impact factor: 49.962

8.  Genomic organization of the adrenoleukodystrophy gene.

Authors:  C O Sarde; J Mosser; P Kioschis; C Kretz; S Vicaire; P Aubourg; A Poustka; J L Mandel
Journal:  Genomics       Date:  1994-07-01       Impact factor: 5.736

9.  Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophy.

Authors:  N Cartier; C O Sarde; A M Douar; J Mosser; J L Mandel; P Aubourg
Journal:  Hum Mol Genet       Date:  1993-11       Impact factor: 6.150

10.  The 70-kDa peroxisomal membrane protein is a member of the Mdr (P-glycoprotein)-related ATP-binding protein superfamily.

Authors:  K Kamijo; S Taketani; S Yokota; T Osumi; T Hashimoto
Journal:  J Biol Chem       Date:  1990-03-15       Impact factor: 5.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.