Natural regulatory mutations elevate the fetal globin gene via disruption of BCL11A or ZBTB7A binding-Reference-Cited by-同舟云学术

Natural regulatory mutations elevate the fetal globin gene via disruption of BCL11A or ZBTB7A binding

Published:2018-04 Issue:4 Volume:50 Page:498-503
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Martyn Gabriella E.,Wienert Beeke,Yang Lu,Shah Manan,Norton Laura J.,Burdach Jon,Kurita Ryo,Nakamura Yukio,Pearson Richard C. M.,Funnell Alister P. W.,Quinlan Kate G. R.,Crossley Merlin^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/s41588-018-0085-0.pdf

Reference53 articles.

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2. Wilber, A., Nienhuis, A. W. & Persons, D. A. Transcriptional regulation of fetal to adult hemoglobin switching: new therapeutic opportunities. Blood 117, 3945–3953 (2011).

3. Fessas, P. & Stamatoyannopoulos, G. Hereditary persistence of fetal hemoglobin in Greece. A study and a comparison. Blood 24, 223–240 (1964).

4. Collins, F. S. et al. A point mutation in the Aγ-globin gene promoter in Greek hereditary persistence of fetal haemoglobin. Nature 313, 325–326 (1985).

5. Oner, R., Kutlar, F., Gu, L. H. & Huisman, T. H. The Georgia type of nondeletional hereditary persistence of fetal hemoglobin has a C→T mutation at nucleotide–114 of the Aγ-globin gene. Blood 77, 1124–1125 (1991).

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