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Volumn 13, Issue 2, 2002, Pages 388-393
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Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome
a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
STEROID;
ADOLESCENT;
ADULT;
ARTICLE;
CHILD;
CHROMOSOME 1Q;
CHROMOSOME MAP;
DISEASE CLASSIFICATION;
FAMILIAL DISEASE;
FEMALE;
FOCAL GLOMERULOSCLEROSIS;
GENE;
GENE MUTATION;
GENETIC ANALYSIS;
HISTOPATHOLOGY;
HUMAN;
INFANT;
KIDNEY FAILURE;
MAJOR CLINICAL STUDY;
MALE;
MINIMAL CHANGE GLOMERULONEPHRITIS;
MOLECULAR CLONING;
NEPHROTIC SYNDROME;
NPHS2 GENE;
PRIORITY JOURNAL;
PROTEINURIA;
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EID: 0036151614
PISSN: 10466673
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (210)
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References (11)
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