Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach-Reference-Cited by-同舟云学术

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

Published:2011-03-20 Issue:4 Volume:43 Page:295-301
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Giardine Belinda,Borg Joseph,Higgs Douglas R,Peterson Kenneth R,Philipsen Sjaak,Maglott Donna,Singleton Belinda K,Anstee David J,Basak A Nazli,Clark Barnaby,Costa Flavia C,Faustino Paula,Fedosyuk Halyna,Felice Alex E,Francina Alain,Galanello Renzo,Gallivan Monica V E,Georgitsi Marianthi,Gibbons Richard J,Giordano Piero C,Harteveld Cornelis L,Hoyer James D,Jarvis Martin,Joly Philippe,Kanavakis Emmanuel,Kollia Panagoula,Menzel Stephan,Miller Webb,Moradkhani Kamran,Old John,Papachatzopoulou Adamantia,Papadakis Manoussos N,Papadopoulos Petros,Pavlovic Sonja,Perseu Lucia,Radmilovic Milena,Riemer Cathy,Satta Stefania,Schrijver Iris,Stojiljkovic Maja,Thein Swee Lay,Traeger-Synodinos Jan,Tully Ray,Wada Takahito,Waye John S,Wiemann Claudia,Zukic Branka,Chui David H K,Wajcman Henri,Hardison Ross C,Patrinos George P

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.785.pdf

Reference33 articles.

1. Anonymous. Human variome microattribution reviews. Nat. Genet. 40, 1 (2008).

2. Patrinos, G.P. & Antonarakis, S.E. Human hemoglobin. in Human Genetics: Problems and Approaches (eds. Speicher, M., Antonarakis, S.E. & Motulsky, A.), 366–401 (Springer-Verlag, Heidelberg, Germany, 2010).

3. Gibbons, R.J., Picketts, D.J., Villard, L. & Higgs, D.R. Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome). Cell 80, 837–845 (1995).

4. Gibbons, R.J. et al. Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS). Nat. Genet. 34, 446–449 (2003).

5. Viprakasit, V. et al. Mutations in the general transcription factor TFIIH result in β-thalassaemia in individuals with trichothiodystrophy. Hum. Mol. Genet. 10, 2797–2802 (2001).

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