Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability

American Journal of Human Genetics

Volumn 91, Issue 1, 2012, Pages 73-82

  Kleefstra, Tjitske ^a,b   Kramer, Jamie M ^a,b,c   Neveling, Kornelia ^a,b   Willemsen, Marjolein H ^a,b   Koemans, Tom S ^a,b,c   Vissers, Lisenka E L M ^a,b   Wissink Lindhout, Willemijn ^a   Fenckova, Michaela ^a,b,c   Van Den Akker, Willem M R ^a,b,c   Kasri, Nael Nadif ^a,b,c   Nillesen, Willy M ^a   Prescott, Trine ^d   Clark, Robin D ^e   Devriendt, Koenraad ^f   Van Reeuwijk, Jeroen ^a,b   De Brouwer, Arjan P M ^a,b,c   Gilissen, Christian ^a,b   Zhou, Huiqing ^a,b,g   Brunner, Han G ^a,b   Veltman, Joris A ^a,b   Schenck, Annette ^a,b,c   Van Bokhoven, Hans ^a,b,c   more..

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c RADBOUD UNIVERSITY   (Netherlands)

^d OSLO UNIVERSITY HOSPITAL   (Norway)

^e LOMA LINDA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f UNIVERSITY OF LEUVEN   (Belgium)

^g RADBOUD UNIVERSITY NIJMEGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMATIN; CLINICAL ARTICLE; CONTROLLED STUDY; DROSOPHILA; EPIGENETICS; EUCHROMATIC HISTONE METHYLTRANSFERASE 1 GENE; FEMALE; GENE; GENE DISRUPTION; GENE MUTATION; GENETIC DISORDER; HUMAN; INTELLECTUAL IMPAIRMENT; KLEEFSTRA SYNDROME; MALE; MBD5 GENE; MIXED LINEAGE LEUKEMIA 3 GENE; NONHUMAN; NR1I3 GENE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SMARCB1 GENE; SMITH MAGENIS SYNDROME;

ANIMALS; CHROMATIN; CHROMOSOMAL PROTEINS, NON-HISTONE; DNA-BINDING PROTEINS; DROSOPHILA; EPIGENESIS, GENETIC; FEMALE; HISTONE-LYSINE N-METHYLTRANSFERASE; HUMANS; INFANT, NEWBORN; INTELLECTUAL DISABILITY; MALE; MUTATION; SYNDROME; TRANSCRIPTION FACTORS;

EID: 84863984610     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2012.05.003     Document Type: Article

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