Mutation analysis of the ATP2A2 gene in Chinese patients with Darier’s disease
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2010.03741.x/fullpdf
Reference7 articles.
1. Mutations in ATP2A2, encoding a Ca2 + pump, cause Darier disease;Sakuntabhai;Nat Genet,1999
2. Novel mutations of the ATP2A2 gene in two families with Darier’s disease;Bing-Jun;Arch Dermatol Res,2009
3. Two novel mutations in the ATP2A2 gene in Chinese patients with Darier disease;Huo;Eur J Dermatol,2009
4. Spectrum of novel ATP2A2 mutations in patients with Darier’s disease;Sakuntabhai;Hum Mol Genet,1999
5. ATP2A2 mutations in Darier’s disease:variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class;Ruiz-Perez;Hum Mol Genet,1999
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1. Three novel mutations of theATP2A2gene in Chinese patients with Darier disease;Australasian Journal of Dermatology;2018-11-18
2. Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease;Human Mutation;2017-02-15
3. Pathology of Intracellular Ca2+;Intracellular Calcium;2014-10-16
4. Bibliography;Intracellular Calcium;2014-10-16
5. Ionic leakage underlies a gain-of-function effect of dominant disease mutations affecting diverse P-type ATPases;Nature Genetics;2013-12-15
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