Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion

Human Molecular Genetics

Volumn 7, Issue 2, 1998, Pages 177-186

  Del Favero, Jurgen ^a   Krols, Luc ^a   Michalik, Andrej ^a   Theuns, Jessie ^a   Löfgren, Ann ^a   Goossens, Dirk ^a   Wehnert, Anita ^a   Van Den Bossche, Dirk ^a   Van Zand, Karel ^a   Backhovens, Hubert ^a   Van Regenmorter, Nicole ^b   Martin, Jean Jacques ^c   Van Broeckhoven, Christine ^a  

^a DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^b FREE UNIVERSITY OF BRUSSELS   (Belgium)

^c UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; CONTIG; DNA MARKER; TRINUCLEOTIDE;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CEREBELLAR ATAXIA; CHROMOSOME 3P; CLINICAL ARTICLE; DNA FLANKING REGION; EXON; FEMALE; GENE; GENE MAPPING; GENE MUTATION; GENE STRUCTURE; HUMAN; HUMAN CELL; MALE; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; ONSET AGE; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RETINA DEGENERATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY; TRINUCLEOTIDE REPEAT; YEAST ARTIFICIAL CHROMOSOME;

ALLELES; BASE SEQUENCE; BELGIUM; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 3; CLONING, MOLECULAR; COSMIDS; DNA, COMPLEMENTARY; FEMALE; GENE EXPRESSION; HUMANS; MACULAR DEGENERATION; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMERASE CHAIN REACTION; SPINOCEREBELLAR DEGENERATIONS; TRINUCLEOTIDE REPEATS;

ATAXIA;

EID: 6844239536     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.2.177     Document Type: Article

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