The sub-nucleolar localization of PHF6 defines its role in rDNA transcription and early processing events
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg201640.pdf
Reference48 articles.
1. Lower KM, Turner G, Kerr BA et al: Mutations in PHF6 are associated with Borjeson-Forssman-Lehmann syndrome. Nat Genet 2002; 32: 661–665.
2. Gecz J, Turner G, Nelson J, Partington M : The Borjeson-Forssman-Lehman syndrome (BFLS, MIM #301900). Eur J Hum Genet 2006; 14: 1233–1237.
3. Van Vlierberghe P, Palomero T, Khiabanian H et al: PHF6 mutations in T-cell acute lymphoblastic leukemia. Nat Genet 2010; 42: 338–342.
4. Van Vlierberghe P, Patel J, Abdel-Wahab O et al: PHF6 mutations in adult acute myeloid leukemia. Leukemia 2011; 25: 130–134.
5. Zweier C, Rittinger O, Bader I et al: Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome. Am J Med Genet C Semin Med Genet 2014; 166C: 290–301.
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