Dynamic mutation: Possible mechanisms and significance in human disease

Trends in Biochemical Sciences

Volumn 22, Issue 11, 1997, Pages 432-436

  Richards, Robert I ^a   Sutherland, Grant R ^a  

^a WOMEN S AND CHILDREN S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA;

DNA SEQUENCE; EPILEPSY; FRAGILE X SYNDROME; GENE CONVERSION; GENETIC DISORDER; GENOTYPE; HUMAN; HUNTINGTON CHOREA; MUTATION; MYOTONIC DYSTROPHY; PHENOTYPE; PRIORITY JOURNAL; REVIEW; TRINUCLEOTIDE REPEAT;

GENETIC DISEASES, INBORN; HUMANS; MUTATION; REPETITIVE SEQUENCES, NUCLEIC ACID;

EID: 0030664357     PISSN: 09680004     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0004(97)01108-0     Document Type: Review

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