Dna analysis in hereditary dentatorubral-pallidoluysian atrophy: Correlation between cag repeat length and phenotypic variation and the molecular basis of anticipation

Neurology

Volumn 45, Issue 1, 1995, Pages 143-149

  Komure, O ^a   Sano, A ^a   Nishino, N ^a   Yamauchi, N ^a   Ueno, S ^a   Kondoh, K ^a   Sano, N ^a   Takahashi, M ^a   Murayama, N ^a   Kondo, I ^a   Nagafuchi, S ^a   Yamada, M ^a   Kanazawa, I ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT DISORDER; BRAIN ATROPHY; BRAIN DEGENERATION; CHOREOATHETOSIS; CHROMOSOME 12P; CLINICAL ARTICLE; DEMENTIA; DISEASE CLASSIFICATION; DISEASE SEVERITY; DNA DETERMINATION; FEMALE; HUMAN; MALE; MYOCLONUS EPILEPSY; PEDIGREE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGE OF ONSET; BASE SEQUENCE; BRAIN; CELL LINE; CHILD; COMPARATIVE STUDY; DNA; DNA PRIMERS; FEMALE; HUMAN; MALE; MIDDLE AGE; MOLECULAR SEQUENCE DATA; MYOCLONIC CEREBELLAR DYSSYNERGIA; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T; VARIATION (GENETICS);

EID: 0028815025     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.45.1.143     Document Type: Article

References (0)