Site and sequence specific DNA methylation in the neurofibromatosis (NF1) gene includes C5839T: The site of the recurrent substitution mutation in exon 31

Human Molecular Genetics

Volumn 5, Issue 4, 1996, Pages 503-507

  Andrews, Joseph D ^b   Mancini, Debora N ^b   Singh, Shiva M ^b   Rodenhiser, David I ^b  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSINE; DINUCLEOTIDE;

ALLELE; ARTICLE; CONTROLLED STUDY; DNA METHYLATION; EXON; GENE MUTATION; GENE SEQUENCE; GERM LINE; HUMAN; HUMAN CELL; MUTAGENESIS; NEUROFIBROMATOSIS; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; SPONTANEOUS MUTATION; SYMPTOM;

BASE SEQUENCE; CYTOSINE; DINUCLEOSIDE PHOSPHATES; DNA; DNA PRIMERS; EXONS; FEMALE; GENES, NEUROFIBROMATOSIS 1; HUMANS; MALE; METHYLATION; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; MUTATION;

EID: 0029880030     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.4.503     Document Type: Article

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