Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome

Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome

Genitopatellar syndrome (GPS) is a skeletal dysplasia with cerebral and genital anomalies for which the molecular basis has not yet been determined. By exome sequencing, we found de novo heterozygous truncating mutations in KAT6B (lysine acetyltransferase 6B, formerly known as MYST4 and MORF) in thr...

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Main Authors: Campeau, Philippe M., Kim, Jaeseung C., Lu, James T., Schwartzentruber, Jeremy A., Abdul-Rahman, Omar A., Schlaubitz, Silke, Murdock, David M., Jiang, Ming-Ming, Lammer, Edward J., Enns, Gregory M., Rhead, William J., Rowland, Jon, Robertson, Stephen P., Cormier-Daire, Valérie, Bainbridge, Matthew N., Yang, Xiang-Jiao, Gingras, Marie-Claude, Gibbs, Richard A., Rosenblatt, David S., Majewski, Jacek, Lee, Brendan H.
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Language:English
Published: Elsevier 2012
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Online Access:https://pmc.ncbi.nlm.nih.gov/articles/PMC3276659/
https://pubmed.ncbi.nlm.nih.gov/22265014
http://dx.doi.org/10.1016/j.ajhg.2011.11.023
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https://pmc.ncbi.nlm.nih.gov/articles/PMC3276659/
https://pubmed.ncbi.nlm.nih.gov/22265014
http://dx.doi.org/10.1016/j.ajhg.2011.11.023

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