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DD is characterized by loss of adhesion between suprabasal epidermal cells associated with abnormal keratinization, while loss of epidermal cell\u2010to\u2010cell adhesion is predominant in HHD. The genes for both conditions have recently been identified using candidate positional cloning approaches. The gene for DD (\n                    <jats:italic>ATP2A2<\/jats:italic>\n                    ) encodes a calcium transport ATPase of the sarco (endo)plasmic reticulum (SERCA2) Verboomen et al. [1992: Biochem J 286(Pt 2):591\u2013595], while the gene for HHD (\n                    <jats:italic>ATP2C1<\/jats:italic>\n                    ) codes for a secretory pathway for calcium and manganese transport ATPase of the Golgi apparatus (SPCA1) Hu et al. [2000: Nat Genet 24:61\u201365]. These results have provided completely new insights into the role of calcium and\/or manganese in maintaining skin integrity. Although the precise disease mechanisms remain to be understood, these discoveries open a new field in research for the understanding and the treatment of these distressing disorders. \u00a9 2004 Wiley\u2010Liss, Inc.\n                  <\/jats:p>","DOI":"10.1002\/ajmg.c.30031","type":"journal-article","created":{"date-parts":[[2004,10,5]],"date-time":"2004-10-05T18:02:16Z","timestamp":1096999336000},"page":"20-31","source":"Crossref","is-referenced-by-count":73,"title":["Calcium pump disorders of the 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