A Novel Small Deletion in the ATP2A2 Gene in a Patient with Sporadic Darier's Disease and Concomitant Depression: A Case Report
Abstract. Introduction:. Darier's disease is a rare autosomal dominant skin disorder caused by mutations in ATP2A2. Recently, the high prevalence of neuropsychiatric symptoms is frequently reported in Darier's disease patients. We present a case of patient with concurrence of Darier's...
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| Main Authors: | , , , , |
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| Format: | Book |
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Wolters Kluwer Health,
2020-09-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |