De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation
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Published:2018-09-17
Issue:10
Volume:50
Page:1442-1451
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ISSN:1061-4036
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Container-title:Nature Genetics
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language:en
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Short-container-title:Nat Genet
Author:
Basilicata M. FeliciaORCID, , Bruel Ange-Line, Semplicio Giuseppe, Valsecchi Claudia Isabelle KellerORCID, Aktaş Tuğçe, Duffourd Yannis, Rumpf Tobias, Morton Jenny, Bache Iben, Szymanski Witold G., Gilissen ChristianORCID, Vanakker Olivier, Õunap Katrin, Mittler Gerhard, van der Burgt Ineke, El Chehadeh Salima, Cho Megan T., Pfundt Rolph, Tan Tiong Yang, Kirchhoff Maria, Menten Björn, Vergult SarahORCID, Lindstrom Kristin, Reis AndréORCID, Johnson Diana S., Fryer Alan, McKay Victoria, Fisher Richard B., Thauvin-Robinet Christel, Francis David, Roscioli Tony, Pajusalu SanderORCID, Radtke Kelly, Ganesh Jaya, Brunner Han G., Wilson Meredith, Faivre Laurence, Kalscheuer Vera M., Thevenon Julien, Akhtar AsifaORCID
Publisher
Springer Science and Business Media LLC
Reference72 articles.
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