Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants-Reference-Cited by-同舟云学术

Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants

Published:2019-04-26 Issue:1 Volume:4 Page:
ISSN:2056-7944
Container-title:npj Genomic Medicine
language:en
Short-container-title:npj Genom. Med.

Author:

Chan Ada J. S.,Cytrynbaum Cheryl^ORCID,Hoang Ny,Ambrozewicz Patricia M.,Weksberg Rosanna,Drmic Irene,Ritzema Anne,Schachar Russell,Walker Susan,Uddin Mohammed,Zarrei Mehdi,Yuen Ryan K. C.^ORCID,Scherer Stephen W.

Funder

Genome Canada

Canada Foundation for Innovation

Canadian Institute for Advanced Research

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

http://www.nature.com/articles/s41525-019-0083-x.pdf

Reference50 articles.

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3. Lim, D. A. et al. Chromatin remodelling factor Mll1 is essential for neurogenesis from postnatal neural stem cells. Nature 458, 529–533 (2009).

4. Krivtsov, A. V. & Armstrong, S. A. MLL translocations, histone modifications and leukaemia stem-cell development. Nat. Rev. Cancer 7, 823–833 (2007).

5. Jones, W. D. et al. De novo mutations in MLL cause Wiedemann-Steiner syndrome. Am. J. Hum. Genet. 91, 358–364 (2012).

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