10662663

Source:http://linkedlifedata.com/resource/pubmed/id/10662663

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0025118, umls-concept:C0025723
pubmed:issue	2
pubmed:dateCreated	2000-3-16
pubmed:abstractText	Two human genetic diseases have recently been shown to be due to mutations in genes encoding proteins involved in DNA methylation. The phenotypes of these two diseases are surprisingly distinct from each other and provide insights into the functions of DNA methylation in mammals.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9107782
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA Modification Methylases
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0960-9822
pubmed:author	pubmed-author:HendrichBB
pubmed:issnType	Print
pubmed:day	27
pubmed:volume	10
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	R60-3
pubmed:dateRevised	2005-11-16
pubmed:meshHeading	pubmed-meshheading:10662663-DNA Methylation, pubmed-meshheading:10662663-DNA Modification Methylases, pubmed-meshheading:10662663-Genetics, Medical, pubmed-meshheading:10662663-Humans, pubmed-meshheading:10662663-Mutation, pubmed-meshheading:10662663-Rett Syndrome, pubmed-meshheading:10662663-Syndrome
pubmed:year	2000
pubmed:articleTitle	Methylation moves into medicine.
pubmed:affiliation	Darwin Building, King's Buildings, Institute of Cell and Molecular Biology, University of Edinburgh, Edinburgh, EH9 3JR, UK. Brian. Hendrich@ed.ac.uk.
pubmed:publicationType	Journal Article, Review