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Volumn 78, Issue 5, 1999, Pages 338-360
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Alport syndrome: An inherited disorder of renal, ocular, and cochlear basement membranes
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Author keywords
[No Author keywords available]
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Indexed keywords
COLLAGEN TYPE 4;
ALPORT SYNDROME;
BASEMENT MEMBRANE;
CLINICAL FEATURE;
COCHLEA;
DIAGNOSTIC APPROACH ROUTE;
EYE;
GENE LOCUS;
GENE MUTATION;
HUMAN;
KIDNEY;
KIDNEY FAILURE;
KIDNEY TRANSPLANTATION;
MOLECULAR GENETICS;
NONHUMAN;
PATHOGENESIS;
PRIORITY JOURNAL;
REVIEW;
SKIN;
ANIMALS;
BASEMENT MEMBRANE;
COCHLEA;
COLLAGEN;
DISEASE MODELS, ANIMAL;
EPIDERMIS;
EYE;
GENE DELETION;
GENE EXPRESSION REGULATION;
GLOMERULOSCLEROSIS, FOCAL SEGMENTAL;
HUMANS;
KIDNEY;
KIDNEY GLOMERULUS;
LEIOMYOMATOSIS;
LINKAGE (GENETICS);
MUTATION;
NEPHRITIS, HEREDITARY;
X CHROMOSOME;
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EID: 0032823921
PISSN: 00257974
EISSN: None
Source Type: Journal
DOI: 10.1097/00005792-199909000-00005 Document Type: Review |
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Times cited : (189)
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References (218)
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