论文信息 - Novel point mutations of the ATP2A2 gene in two Chinese families with Darier disease. - 字舞流文

Novel point mutations of the ATP2A2 gene in two Chinese families with Darier disease.

Y. Yang | D. Bu | G. Li | X. Zhu | X. Zhu

[1] T. Strachan,et al. ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class. , 1999, Human molecular genetics.

[2] N. Craddock,et al. ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes. , 1999, Human molecular genetics.

[3] N. Craddock,et al. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease , 1999, Nature Genetics.

[4] R. O. Stuart,et al. Dependence of Epithelial Intercellular Junction Biogenesis on Thapsigargin-sensitive Intracellular Calcium Stores* , 1996, The Journal of Biological Chemistry.

[5] J. Wilkinson,et al. Darier-White disease: a review of the clinical features in 163 patients. , 1992, Journal of the American Academy of Dermatology.

[6] J. Lytton,et al. Molecular cloning of cDNAs from human kidney coding for two alternatively spliced products of the cardiac Ca2+-ATPase gene. , 1988, The Journal of biological chemistry.