Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease
Mutations in KDM5C gene are linked to X-linked mental retardation, the syndromic Claes-Jensen-type disease. This study focuses on non-synonymous mutations in the KDM5C ARID domain and evaluates the effects of two disease-associated missense mutations (A77T and D87G) and three not-yet-classified miss...
Main Authors: | Yunhui Peng, Jimmy Suryadi, Ye Yang, Tugba G. Kucukkal, Weiguo Cao, Emil Alexov |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2015-11-01
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Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | http://www.mdpi.com/1422-0067/16/11/26022 |
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