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Volumn 293, Issue 5531, 2001, Pages 864-867
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Myotonic dystrophy type 2 caused by a CCTG expansion in intron I of ZNF9
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Author keywords
[No Author keywords available]
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Indexed keywords
CHROMOSOMES;
PROTEINS;
RNA;
MUSCULAR DYSTROPHY (DM);
GENE TRANSFER;
CHROMOSOME;
DISEASE;
MUTATION;
ARTICLE;
CHROMOSOME 19Q;
CHROMOSOME 3Q;
FAMILY STUDY;
GENE MUTATION;
HAPLOTYPE;
HUMAN;
MAJOR CLINICAL STUDY;
MUSCULAR DYSTROPHY;
MYOTONIC DYSTROPHY;
PHENOTYPE;
PRIORITY JOURNAL;
TRINUCLEOTIDE REPEAT;
ALLELES;
BLOTTING, SOUTHERN;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 3;
DISEASES IN TWINS;
DNA-BINDING PROTEINS;
FEMALE;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
INTRONS;
LINKAGE DISEQUILIBRIUM;
LOD SCORE;
MALE;
MICROSATELLITE REPEATS;
MUSCLES;
MUTATION;
MYOTONIC DYSTROPHY;
PHENOTYPE;
POLYMERASE CHAIN REACTION;
RNA, MESSENGER;
RNA-BINDING PROTEINS;
TWINS, MONOZYGOTIC;
ZINC FINGERS;
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EID: 0035800434
PISSN: 00368075
EISSN: None
Source Type: Journal
DOI: 10.1126/science.1062125 Document Type: Article |
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Times cited : (1066)
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References (49)
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