A Role for Non-B DNA Forming Sequences in Mediating Microlesions Causing Human Inherited Disease

Human Mutation

Volumn 37, Issue 1, 2016, Pages 65-73

  Kamat, Mihir Anant ^a,c   Bacolla, Albino ^b   Cooper, David N ^b   Chuzhanova, Nadia ^a  

^a NOTTINGHAM TRENT UNIVERSITY   (United Kingdom)

^b CARDIFF UNIVERSITY   (United Kingdom)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

Mechanisms of mutagenesis; Microdeletions; Microinsertions; Missense mutations; Non B DNA; Nonsense mutations

Indexed keywords

DNA B; GUANINE QUADRUPLEX;

ARTICLE; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; DNA CONFORMATION; DNA REPAIR; DNA REPLICATION; DNA SEQUENCE; DNA STRAND BREAKAGE; DNA TEMPLATE; EXCISION REPAIR; GENE DELETION; GENE INSERTION; GENETIC DISORDER; HUMAN; INVERTED REPEAT; MISSENSE MUTATION; MUTAGENESIS; NONSENSE MUTATION; NUCLEIC ACID BASE SUBSTITUTION; OXIDATION; PRIORITY JOURNAL; BIOLOGY; CHEMISTRY; CONFORMATION; GENE EXPRESSION REGULATION; GENETIC ASSOCIATION STUDY; GENETIC DATABASE; GENETICS; INFORMATION PROCESSING; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE;

BASE SEQUENCE; COMPUTATIONAL BIOLOGY; DATABASES, GENETIC; DATASETS AS TOPIC; DNA, B-FORM; GENETIC ASSOCIATION STUDIES; GENETIC DISEASES, INBORN; HUMANS; MUTAGENESIS, INSERTIONAL; NUCLEIC ACID CONFORMATION; REPETITIVE SEQUENCES, NUCLEIC ACID; SEQUENCE DELETION;

EID: 84954361314     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22917     Document Type: Article

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