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Volumn 50, Issue 6, 1992, Pages 1291-1300
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Mutation in the α5(IV) collagen chain in juvenile-onset Alport syndrome without hearing loss or ocular lesions: Detection by denaturing gradient gel electrophoresis of a PCR product
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Author keywords
[No Author keywords available]
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Indexed keywords
COLLAGEN TYPE 4;
DNA;
ADULT;
AGED;
ALPHA CHAIN;
ALPORT SYNDROME;
ARTICLE;
CASE REPORT;
CLINICAL FEATURE;
CONTROLLED STUDY;
DENSITY GRADIENT;
DNA SEQUENCE;
ELECTRON MICROSCOPY;
EXON;
FEMALE;
GEL ELECTROPHORESIS;
GENE AMPLIFICATION;
GENE MUTATION;
GLOMERULUS BASEMENT MEMBRANE;
HUMAN;
MALE;
ONSET AGE;
PEDIGREE;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
RESTRICTION SITE;
SOUTHERN BLOTTING;
X CHROMOSOME LINKAGE;
ADULT;
AMINO ACID SEQUENCE;
BASE SEQUENCE;
BASEMENT MEMBRANE;
CASE REPORT;
COLLAGEN;
DNA;
ELECTROPHORESIS, POLYACRYLAMIDE GEL;
EXONS;
EYE DISEASES;
FEMALE;
HEARING DISORDERS;
HUMAN;
MACROMOLECULAR SYSTEMS;
MALE;
MICROSCOPY, ELECTRON;
MOLECULAR SEQUENCE DATA;
NEPHRITIS, HEREDITARY;
OLIGODEOXYRIBONUCLEOTIDES;
PEDIGREE;
POLYMERASE CHAIN REACTION;
RESTRICTION MAPPING;
SUPPORT, NON-U.S. GOV'T;
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EID: 0026631416
PISSN: 00029297
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (49)
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References (0)
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