A genome-wide DNA methylation signature for SETD1B-related syndrome

<div><p>SETD1B is a component of a histone methyltransferase complex that specifically methylates Lys-4 of histone H3 (H3K4) and is responsible for the epigenetic control of chromatin structure and gene expression. De novo microdeletions encompassing this gene as well as de novo missense...

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التفاصيل البيبلوغرافية
المؤلف الرئيسي:	I. M. Krzyzewska (18614968) (author)
مؤلفون آخرون:	S. M. Maas (18614971) (author), P. Henneman (5044997) (author), K. v. d. Lip (18614974) (author), A. Venema (5044994) (author), K. Baranano (7819424) (author), A. Chassevent (7819427) (author), E. Aref-Eshghi (7819430) (author), A. J. van Essen (18614977) (author), T. Fukuda (7819436) (author), H. Ikeda (2235205) (author), M. Jacquemont (7819439) (author), H.-G. Kim (7819442) (author), A. Labalme (3807079) (author), S. M. E. Lewis (18614980) (author), G. Lesca (3807094) (author), I. Madrigal (7819445) (author), S. Mahida (7819448) (author), N. Matsumoto (7819451) (author), R. Rabionet (7819454) (author), E. Rajcan-Separovic (7819457) (author), Y. Qiao (6511862) (author), B. Sadikovic (7819460) (author), H. Saitsu (7819463) (author), D. A. Sweetser (18614983) (author), M. Alders (6496589) (author), M. M. A. M. Mannens (18614986) (author)
منشور في:	2019
الموضوعات:	Biological sciences Genetics Epigenetic control Chromatin structure Gene expression Microdeletions Missense mutations Syndromic intellectual disability (ID)
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A genome-wide DNA methylation signature for SETD1B-related syndrome

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