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Volumn 14, Issue 6, 2000, Pages 502-512

Alport syndromes: Phenotypic heterogeneity of progressive hereditary nephritis

Author keywords

Alport syndrome; Extrarenal disease; Heterogeneity; Molecular genetics

Indexed keywords

ALPORT SYNDROME; BASEMENT MEMBRANE; BIOCHEMISTRY; FEMALE; GENETIC HETEROGENEITY; HUMAN; MALE; MOLECULAR GENETICS; NEPHRITIS; NEUROPATHY; NONHUMAN; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; REVIEW; ULTRASTRUCTURE;

EID: 0034110693     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004670050804     Document Type: Review
Times cited : (50)

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