CpG methylation accounts for a recurrent mutation (c.1222C>T) in the human PAH gene.

Human mutation

Volumn 27, Issue 9, 2006, Pages 975-

  Murphy, B C ^a   Scriver, C R ^a   Singh, S M ^a  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

ALLELE; ANIMAL; ARTICLE; CPG ISLAND; DNA METHYLATION; EXON; GENE FREQUENCY; GENETICS; HUMAN; MACACA; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PAN TROGLODYTES; PAPIO; PHENYLKETONURIA; POINT MUTATION;

ALLELES; ANIMALS; BASE SEQUENCE; CPG ISLANDS; DNA METHYLATION; DNA MUTATIONAL ANALYSIS; EXONS; GENE FREQUENCY; HUMANS; MACACA FASCICULARIS; MOLECULAR SEQUENCE DATA; PAN TROGLODYTES; PAPIO; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIAS; POINT MUTATION;

EID: 33750584291     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9447     Document Type: Article

References (0)