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CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene
Author(s) -
Murphy B.C.,
Scriver C.R.,
Singh S.M.
Publication year - 2006
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.9447
Subject(s) - biology , genetics , exon , allele , locus (genetics) , cpg site , haplotype , gene , dna methylation , gene expression
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