Dominantly inherited, non-coding microsatellite expansion disorders

Current Opinion in Genetics and Development

Volumn 12, Issue 3, 2002, Pages 266-271

  Ranum, Laura P W ^a   Day, John W ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; PHOSPHOPROTEIN PHOSPHATASE 2A; PROTEIN; PROTEIN ZNF9; RNA; UNCLASSIFIED DRUG; MICROSATELLITE DNA;

3' UNTRANSLATED REGION; CLINICAL FEATURE; HUMAN; HUNTINGTON CHOREA; MOLECULAR BIOLOGY; MUTATION; MYOTONIC DYSTROPHY; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN FUNCTION; REVIEW; SPINOCEREBELLAR DEGENERATION; DOMINANT GENE; GENETIC DISORDER; GENETICS; PHENOTYPE; TRINUCLEOTIDE REPEAT;

ATAXIA;

GENES, DOMINANT; GENETIC DISEASES, INBORN; HUMANS; HUNTINGTON DISEASE; MICROSATELLITE REPEATS; MYOTONIC DYSTROPHY; PHENOTYPE; RNA; SPINOCEREBELLAR ATAXIAS; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 0036591663     PISSN: 0959437X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-437X(02)00297-6     Document Type: Review

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