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[2] Bashir R, Munro CS, Mason S, et al. Localisation of a gene for Darier's disease. Hum Mol Genet, 1993, 2:1937-1939.
[3] Craddock N, Dawson E, Burge S, et al. The gene for Darier's disease maps to chromosome 12q23-q24.1. Hum Mol Genet, 1993,2:1941-1943.
[4] Parfitt E, Burge S, Craddock N, et al. The gene for Darier's disease maps between D12S78 and D12S79. Hum Mol Genet, 1994, 3:35-38.
[5] Carter SA, Bryce SD, Munro CS, et al. Linkage analyses in British pedigrees suggest a single locus for Darier disease and narrow the location to the interval between D12S105 and D12S129. Genomics,1994, 24:378-382.
[6] Kennedy JL, Berg D, Bassett AS, et al. Genetic linkage for Darier disease (keratosis follicularis). Am J Med Genet, 1995, 55:307-310.
[7] Ikeda S, Shigihara T, Ogawa H, et al. Narrowing of the Darier disease gene interval on chromosome 12q. J Invest Dermatol, 1998,110:847-848.
[8] Sakuntabhai A, Ruiz-Perez V, Carter S, et al. Mutations in ATP2A2, encoding a Ca2 + pump, cause Darier disease. Nat Genet, 1999, 21:271-277.
[9] Cooper SM, Burge SM. Darier's disease: epidemiology, pathophysiology, and management. Am J Clin Dermatol, 2003, 4:97-105.
[10] Zhao XS, Shin DM, Liu LH, et al. Plasticity and adaptation of Ca2 +signaling and Ca2 +-dependent exocytosis in SERCA2(+/-) mice.EMBO J, 2001,20:2680-2689.
[11] Sakuntabhai A, Burge S, Monk S, et al. Spectrum of novel ATP2A2mutations in patients with Darier's disease. Hum Mol Genet, 1999,8:1611-1619.
[12] Dhitavat J, Dode L, Leslie N,et al. Mutations in the sarcoplasmic/endoplasmic reticulum Ca2 + ATPase isoform cause Darier's disease.J Invest Dermatol, 2003, 121:486-489.
[13] Ahn W, Lee MG, Kim KH, et al. Multiple effects of SERCA2b mutations associated with Darier's disease. J Biol Chem, 2003, 278:20795-20801.
[14] Pecina-Slaus N, Milavec-Puretic V, Kubat M, et al. Clinical case of acral hemorrhagic Darier's disease is not caused by mutations in exon
[15] of the ATP2A2 gene. Coll Antropol, 2003, 27:125-133.15.Inada M, Shimizu H, Yamada S, et al. Three cases of Darier's disease in a family showing marked heterogeneous clinical severity. Dermatology, 1999, 198:167-170.
[16] Ringpfeil F, Raus A, DiGiovanna JJ, et al. Darier disease-novel mutations in ATP2A2 and genotype-phenotype correlation. Exp Dermatol, 2001, 10:19-27.
[17] Yang S, Sun LD, Liu HS, et al. A novel missense mutation of the ATP2A2 gene in a Chinese family with Darier's disease. Arch Dermatol Res, 2004, 296:21-24.
[18] Racz E, Csikos M, Kornsee Z, et al. Identification of mutations in the ATP2A2 gene in patients with Darier's disease from Hungary. Exp Dermatol, 2004, 13:396-399.
[19] Wada T, Shirakata Y, Takahashi H, et al. A Japanese case of segmental Darier's disease caused by mosaicism for the ATP2A2 mutation. Br J Dermatol, 2003, 149:185-188.
[20] Sakuntabhai A, Dhitavat J, Burge S, et al. Mosaicism for ATP2A2mutations causes segmental Darier's disease. J Invest Dermatol,2000, 115:1144-1147.
[21] Petros AM, Olejniczak ET, Fesik SW. Structural biology of the Bcl-2 family of proteins. Biochim Biophys Acta, 2004,1644:83-94.
[22] Bongiorno MR, Arico M. The behaviour of Bcl-2, Bax and Bcl-x in Darier's disease. Br J Dermatol, 2002, 147:696-700.