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Volumn 41, Issue 11, 2000, Pages 3278-3285
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A new βA1-crystallin splice junction mutation in autosomal dominant cataract
a
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Author keywords
[No Author keywords available]
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Indexed keywords
CRYSTALLIN;
PRIMER DNA;
ADULT;
ARTICLE;
AUTOSOMAL DOMINANT DISORDER;
BRAZIL;
CATARACT;
CHROMOSOME 17Q;
CLINICAL ARTICLE;
CLINICAL EXAMINATION;
DNA POLYMORPHISM;
DNA SEQUENCE;
GENE MAPPING;
GENE MUTATION;
GENETIC LINKAGE;
HUMAN;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
CHEMISTRY;
CHROMOSOME 17;
CHROMOSOME MAP;
EYE DISEASE;
FEMALE;
GENETIC MARKER;
GENETIC POLYMORPHISM;
GENETICS;
MALE;
MOLECULAR GENETICS;
MUTATION;
NUCLEOTIDE SEQUENCE;
PEDIGREE;
RNA SPLICING;
BASE SEQUENCE;
CATARACT;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 17;
CRYSTALLINS;
DNA PRIMERS;
EYE DISEASES, HEREDITARY;
FEMALE;
GENETIC MARKERS;
HUMANS;
LINKAGE (GENETICS);
LOD SCORE;
MALE;
MOLECULAR SEQUENCE DATA;
MUTATION;
PEDIGREE;
POLYMERASE CHAIN REACTION;
POLYMORPHISM, GENETIC;
RNA SPLICING;
SEQUENCE ANALYSIS, DNA;
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EID: 0033623351
PISSN: 01460404
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (81)
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References (70)
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