Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?
Author:
Funder
Telethon Network of Genetic Biobanks
EuroBioBank
NINDS Informatics Center
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference10 articles.
1. Choreoathetosis, congenital hypothyroidism and neonatal respiratory distress syndrome with intact NKX2-1;Barnett;Am. J. Med. Genet.,2012
2. Mutations in TITF-1 are associated with benign hereditary chorea;Breedveld;Hum. Mol. Genet.,2002
3. Chromatin domains: the unit of chromosome organization;Dixon;Mol. Cell.,2016
4. The 3D genome in transcriptional regulation and pluripotency;Gorkin;Cell Stem Cell.,2014
5. A further case of brain-lung-thyroid syndrome with deletion proximal to NKX2-1;Kharbanda;Eur. J. Med. Genet.,2017
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