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

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...

وصف كامل

محفوظ في:
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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