Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns

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Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns.

CHD7 is a member of the chromodomain helicase DNA binding domain family of ATP-dependent chromatin remodeling enzymes. De novo mutation of the CHD7 gene is a major cause of CHARGE syndrome, a genetic disease characterized by a complex constellation of birth defects (Coloboma of the eye, Heart defects, Atresia of the choanae, severe Retardation of growth and development, Genital abnormalities, a...

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ژورنال

عنوان ژورنال: Genome Research

سال: 2009

ISSN: 1088-9051

DOI: 10.1101/gr.086983.108