Wilson's disease (WD), an autosomal recessive disorder of copper transport with a broad range of genotypic and phenotypic characteristics, results from mutations in the ATP7B gene. Herein we report the results of mutation analysis of the ATP7B gene in a group of 118 Wilson disease families (236 chromosomes) prevalently of Italian origin. Using DNA sequencing we identified 83 disease-causing mutations. Eleven were novel, while twenty one already described mutations were identified in new populations in this study. In particular, mutation analysis of 13 families of Romanian origin showed a high prevalence of the p.H1069Q mutation (50%). Detection of new mutations in the ATP7B gene in new populations increases our capability of molecular analysis that is essential for early diagnosis and treatment of WD. (C) 2012 Elsevier Ltd. All rights reserved.
Mutation analysis of the ATP7B gene in a new group of Wilson's disease patients: Contribution to diagnosis / Maria Barbara, Lepori; Antonietta, Zappu; Simona, Incollu; Valentina, Dessi; Eva, Mameli; Luigi, Demelia; Anna Maria, Nurchi; Liana, Gheorghe; Giuseppe, Maggiore; Marco, Sciveres; Leuzzi, Vincenzo; Giuseppe, Indolfi; Luisa, Bonafe; Casali, Carlo; Paolo, Angeli; Patrizia, Barone; Antonio, Cao; Georgios, Loudianos. - In: MOLECULAR AND CELLULAR PROBES. - ISSN 0890-8508. - ELETTRONICO. - 26:4(2012), pp. 147-150. [10.1016/j.mcp.2012.03.007]
Mutation analysis of the ATP7B gene in a new group of Wilson's disease patients: Contribution to diagnosis
LEUZZI, Vincenzo;CASALI, Carlo;
2012
Abstract
Wilson's disease (WD), an autosomal recessive disorder of copper transport with a broad range of genotypic and phenotypic characteristics, results from mutations in the ATP7B gene. Herein we report the results of mutation analysis of the ATP7B gene in a group of 118 Wilson disease families (236 chromosomes) prevalently of Italian origin. Using DNA sequencing we identified 83 disease-causing mutations. Eleven were novel, while twenty one already described mutations were identified in new populations in this study. In particular, mutation analysis of 13 families of Romanian origin showed a high prevalence of the p.H1069Q mutation (50%). Detection of new mutations in the ATP7B gene in new populations increases our capability of molecular analysis that is essential for early diagnosis and treatment of WD. (C) 2012 Elsevier Ltd. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
