Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E

Epigenetics

Volumn 9, Issue 8, 2014, Pages 1184-1193

  Sun, Zhifu ^a   Wu, Yanhong ^a   Ordog, Tamas ^a,b   Baheti, Saurabh ^a   Nie, Jinfu ^a   Duan, Xiaohui ^a   Hojo, Kaori ^c   Kocher, Jean Pierre ^a   Dyck, Peter J ^a   Klein, Christopher J ^a  

^a MAYO CLINIC   (United States)

^b MAYO GRADUATE SCHOOL   (United States)

^c Harima Institute   (Japan)

Author keywords

DNA methylation; HSAN1E; Neurodegeneration; OMIM 604121; OMIM 614116; Whole genome bisulfite sequencing

Indexed keywords

DNA (CYTOSINE 5) METHYLTRANSFERASE; DNA (CYTOSINE-5-)-METHYLTRANSFERASE 1; HISTONE; NICOTINAMIDE ADENINE DINUCLEOTIDE;

CHROMOSOME 18; CPG ISLAND; DNA METHYLATION; DNA SEQUENCE; GENETICS; GENOME IMPRINTING; HUMAN; METABOLISM; MITOCHONDRIAL GENE; MUTATION; NEUROPATHY; PRESCHOOL CHILD; PROTEIN PROCESSING; X CHROMOSOME;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, X; CPG ISLANDS; DNA (CYTOSINE-5-)-METHYLTRANSFERASE; DNA METHYLATION; GENES, MITOCHONDRIAL; GENOMIC IMPRINTING; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HISTONES; HUMANS; MUTATION; NAD; PROTEIN PROCESSING, POST-TRANSLATIONAL; SEQUENCE ANALYSIS, DNA;

EID: 84905638292     PISSN: 15592294     EISSN: 15592308     Source Type: Journal    
DOI: 10.4161/epi.29676     Document Type: Article

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