Biallelic HMGXB4 loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features
Author:
Funder
King Abdullah International Medical Research Center
Publisher
Elsevier BV
Reference19 articles.
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2. HMGB proteins and transcriptional regulation;Ueda;Biochim. Biophys. Acta,2010
3. HMGB proteins: interactions with DNA and chromatin;Stros;Biochim. Biophys. Acta,2010
4. Biological functions and theranostic potential of HMGB family members in human cancers;Niu;Ther Adv Med Oncol,2020
5. HMG box transcription factor TCF-4's interaction with CtBP1 controls the expression of the Wnt target Axin2/Conductin in human embryonic kidney cells;Valenta;Nucleic Acids Res.,2003
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