Two novel missense mutations of ATP2A2 in two Chinese patients with sporadic Darier Disease

Summary Darier disease (DD) is a rare autosomal dominant skin disorder with characteristic abnormal keratinization and acantholysis. The causative gene, ATP2A2, is located on chromosome 12, and encodes a sarco/endoplasmic reticulum calcium pump ATPase (SERCA2). Two Chinese patients with sporadic DD...

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Veröffentlicht in:	Clinical and experimental dermatology 2015-03, Vol.40 (2), p.201-203
Hauptverfasser:	Liang, Y. H., Zhang, Q. G., Liu, Q. X.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Darier Disease - genetics Humans Male Middle Aged Mutation Mutation, Missense Sarcoplasmic Reticulum Calcium-Transporting ATPases - genetics
Online-Zugang:	Volltext
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