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

Williams–Beuren syndrome (also known as Williams syndrome) is caused by a deletion of a 1.55- to 1.84-megabase region from chromosome band 7q11.23. GTF2IRD1 and GTF2I, located within this critical region, encode proteins of the TFII-I family with multiple helix–loop–helix domains known as I repeats....

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Detaylı Bibliyografya
Yayımlandı:Proc Natl Acad Sci U S A
Asıl Yazarlar: Makeyev, Aleksandr V., Erdenechimeg, Lkhamsuren, Mungunsukh, Ognoon, Roth, Jutta J., Enkhmandakh, Badam, Ruddle, Frank H., Bayarsaihan, Dashzeveg
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2004
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC503739/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15243160/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.0404150101
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