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Updated: Jun 23, 2025

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
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A novel ATP2A2 mutation in a familial case of Darier disease accompanied with intellectual disability
1Department of Endocrinology, The Second Hospital of Dalian Medical University, Dalian, China.
The Journal of Dermatology
|June 19, 2024
Abstract
No abstract available in PubMed .
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