GTF2IRD2 is located in the Williams-Beuren syndrome critical region 7q11.23 and encodes a protein with two TFII-I-like helix-loop-helix repeats
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference25 articles.
1. Williams-Beuren syndrome: a challenge for genotype-phenotype correlations
2. Williams Syndrome: 15 Years of Psychological Research
3. Biochemistry and biology of the inducible multifunctional transcription factor TFII-I
4. A Mouse Single-Copy Gene,Gtf2i,the Homolog of HumanGTF2I,That Is Duplicated in the Williams–Beuren Syndrome Deletion Region
5. A duplicated gene in the breakpoint regions of the 7q11.23 Williams- Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK
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