EMBO Workshop Report, Hammersmith Hospital, April 1-3 1998: Trinucleotide expansion diseases in the context of micro- and minisatellite evolution

EMBO Journal

Volumn 17, Issue 19, 1998, Pages 5521-5524

  Hancock, John M ^a   Santibáñez Koref, Mauro F ^a  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA; TRINUCLEOTIDE;

CONFERENCE PAPER; GENE MUTATION; GENETIC DISORDER; HUMAN; HUMAN CELL; MOLECULAR EVOLUTION; MOLECULAR GENETICS; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT; CHROMOSOME ABERRATION; CHROMOSOME DISORDER; FRAGILE X SYNDROME; GENETICS; MUSCLE ATROPHY; MUTAGENESIS; MYOTONIC DYSTROPHY;

CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; EVOLUTION, MOLECULAR; FRAGILE X SYNDROME; HUMANS; MUSCULAR ATROPHY; MUTAGENESIS; MYOTONIC DYSTROPHY; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 0345487521     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1093/emboj/17.19.5521     Document Type: Conference Paper

References (2)

1. Kremer, E.J., Pritchard, M., Lynch, M., Yu, S., Holman, K., Baker, E., Warren, S.T., Schlessinger, D., Sutherland, G.R. and Richards, R.I. (1991). Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n. Science, 252, 1711-1714.
2. La Spada, A.R., Wilson, E.M. Lubahn, D.B., Harding, A.E. and Fischbeck, K.H. (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature, 352, 77-79.