Evidence for further genetic heterogeneity in nephronophthisis

Nephrology Dialysis Transplantation

Volumn 16, Issue 4, 2001, Pages 755-758

  Omran, Heymut ^a   Häffner, Karsten ^a   Burth, Suse ^a   Ala Mello, Sirpa ^b   Antignac, Corinne ^c   Hildebrandt, Friedhelm ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

^b UNIVERSITY OF HELSINKI   (Finland)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Chronic renal failure; Linkage analysis; Nephronophthisis; NPHP1; NPHP3

Indexed keywords

MICROSATELLITE DNA;

ADOLESCENT; ADULT; AGE; ANAMNESIS; ARTICLE; BASEMENT MEMBRANE; CHILD; CHROMOSOME 2Q; CHROMOSOME 3Q; CLINICAL FEATURE; CONTROLLED STUDY; CYST; DISEASE CLASSIFICATION; ENURESIS; EVALUATION; FAMILY; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC HETEROGENEITY; GENETIC LINKAGE; HAPLOTYPE; HISTOPATHOLOGY; HUMAN; INTERSTITIAL NEPHRITIS; KIDNEY DISEASE; KIDNEY FAILURE; KIDNEY TUBULE; MALE; NEPHRONOPHTHISIS; POLYDIPSIA; POLYURIA; PRIORITY JOURNAL; PROGENY; VENEZUELA;

EID: 0035081090     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/16.4.755     Document Type: Article

References (18)

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