Identification of Several Mutations in ATP2C1 in Lebanese Families: Insight into the Pathogenesis of Hailey-Hailey Disease

Author:

Btadini Waed,Abou Hassan Ossama K.,Saadeh Dana,Abbas Ossama,Ballout Farah,Kibbi Abdul-Ghani,Dbaibo Ghassan,Darwiche Nadine,Nemer Georges,Kurban Mazen

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference19 articles.

1. FAMILIAL BENIGN CHRONIC PEMPHIGUS;H HAILEY;Arch Dermatol,1939

2. Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump;R Sudbrak;Hum Mol Genet,2000

3. The role of the Golgi-resident SPCA Ca2+/Mn2+ pump in ionic homeostasis and neural function;W He;Neurochem Res,2012

4. Human keratinocyte ATP2C1 localizes to the Golgi and controls Golgi Ca2+ stores;MJ Behne;J Invest Dermatol,2003

5. Desmosomes: interconnected calcium-dependent structures of remarkable stability with significant integral membrane protein turnover;R Windoffer;J Cell Sci,2002

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