Literature DB >> 16297192

ATP2C1 gene mutation analysis in Italian patients with Hailey-Hailey disease.

Silvia Majore1, Gianfranco Biolcati, Luana Barboni, Carlo Cannistraci, Francesco Binni, Alessandra Crisi, Mauro Picardo, Paola Grammatico.   

Abstract

Hailey-Hailey disease (HHD) is a rare autosomal dominant disorder characterized by recurrent skin lesions predominantly involving the body folds. It is caused by heterozygous mutations in the ATP2C1 gene, encoding the human secretory pathway Ca2+/Mn2+-ATPase protein 1 (hSPCA1). In this report we describe the molecular studies performed in eight HHD cases from Italy that led us to identify six different mutations scattered through the ATP2C1 gene in seven of eight cases. Four of the detected mutations were novel. Our results confirm the high allelic heterogeneity of the ATP2C1 gene and support the notion that HHD is a genetically homogeneous disorder. Furthermore, we created a table summarizing all previously reported ATP2C1 mutations, adapting the nomenclature, if needed, according to the guidelines of the Human Genome Variation Society.

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Year:  2005        PMID: 16297192     DOI: 10.1111/j.0022-202X.2005.23941.x

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  1 in total

Review 1.  ATP2C1 gene mutations in Hailey-Hailey disease and possible roles of SPCA1 isoforms in membrane trafficking.

Authors:  M Micaroni; G Giacchetti; R Plebani; G G Xiao; L Federici
Journal:  Cell Death Dis       Date:  2016-06-09       Impact factor: 8.469

  1 in total

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