Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms-Reference-Cited by-同舟云学术

Somatic PHF6 mutations in 1760 cases with various myeloid neoplasms

Published:2016-08-01 Issue:11 Volume:30 Page:2270-2273
ISSN:0887-6924
Container-title:Leukemia
language:en
Short-container-title:Leukemia

Author:

Mori T,Nagata Y,Makishima H,Sanada M,Shiozawa Y,Kon A,Yoshizato T,Sato-Otsubo A,Kataoka K^ORCID,Shiraishi Y,Chiba K,Tanaka H,Ishiyama K,Miyawaki S,Mori H,Nakamaki T,Kihara R,Kiyoi H,Koeffler H P,Shih L-Y,Miyano S,Naoe T,Haferlach C,Kern W,Haferlach T,Ogawa S,Yoshida K

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Link

http://www.nature.com/articles/leu2016212.pdf

Reference15 articles.

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2. Lower KM, Turner G, Kerr BA, Mathews KD, Shaw MA, Gedeon AK et al. Mutations in PHF6 are associated with Borjeson-Forssman-Lehmann syndrome. Nat Genet 2002; 32: 661–665.

3. Borjeson M, Forssman H, Lehmann O . An X-linked, recessively inherited syndrome characterized by grave mental deficiency, epilepsy, and endocrine disorder. Acta Med Scand 1962; 171: 13–21.

4. Wieczorek D, Bogershausen N, Beleggia F, Steiner-Haldenstatt S, Pohl E, Li Y et al. A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling. Hum Mol Genet 2013; 22: 5121–5135.

5. Van Vlierberghe P, Palomero T, Khiabanian H, Van der Meulen J, Castillo M, Van Roy N et al. PHF6 mutations in T-cell acute lymphoblastic leukemia. Nat Genet 2010; 42: 338–342.

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