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De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation

(2018) Nature Genetics. 50(10). p.1442-1451
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Chicago
Basilicata, M. Felicia, Ange-Line Bruel, Giuseppe Semplicio, Claudia Isabelle Keller Valsecchi, Tuğçe Aktaş, Yannis Duffourd, Tobias Rumpf, et al. 2018. “De Novo Mutations in MSL3 Cause an X-linked Syndrome Marked by Impaired Histone H4 Lysine 16 Acetylation.” Nature Genetics 50 (10): 1442–1451.
APA
Basilicata, M. F., Bruel, A.-L., Semplicio, G., Valsecchi, C. I. K., Aktaş, T., Duffourd, Y., Rumpf, T., et al. (2018). De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. Nature Genetics, 50(10), 1442–1451.
Vancouver
1.
Basilicata MF, Bruel A-L, Semplicio G, Valsecchi CIK, Aktaş T, Duffourd Y, et al. De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. Nature Genetics. Springer Nature; 2018;50(10):1442–51.
MLA
Basilicata, M. Felicia et al. “De Novo Mutations in MSL3 Cause an X-linked Syndrome Marked by Impaired Histone H4 Lysine 16 Acetylation.” Nature Genetics 50.10 (2018): 1442–1451. Print.
@article{8607998,
  author       = {Basilicata, M. Felicia and Bruel, Ange-Line and Semplicio, Giuseppe and Valsecchi, Claudia Isabelle Keller and Akta\c{s}, Tu\u{g}\c{c}e and Duffourd, Yannis and Rumpf, Tobias and Morton, Jenny and Bache, Iben and Szymanski, Witold G. and Gilissen, Christian and Vanakker, Olivier and {\~O}unap, Katrin and Mittler, Gerhard and van der Burgt, Ineke and El Chehadeh, Salima and Cho, Megan T. and Pfundt, Rolph and Tan, Tiong Yang and Kirchhoff, Maria and Menten, Bj{\"o}rn and Vergult, Sarah and Lindstrom, Kristin and Reis, Andr{\'e} and Johnson, Diana S. and Fryer, Alan and McKay, Victoria and Fisher, Richard B. and Thauvin-Robinet, Christel and Francis, David and Roscioli, Tony and Pajusalu, Sander and Radtke, Kelly and Ganesh, Jaya and Brunner, Han G. and Wilson, Meredith and Faivre, Laurence and Kalscheuer, Vera M. and Thevenon, Julien and Akhtar, Asifa},
  issn         = {1061-4036},
  journal      = {Nature Genetics},
  language     = {eng},
  number       = {10},
  pages        = {1442--1451},
  publisher    = {Springer Nature},
  title        = {De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation},
  url          = {http://dx.doi.org/10.1038/s41588-018-0220-y},
  volume       = {50},
  year         = {2018},
}

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