Improved strategy for molecular genetic diagnostics in Juvenile nephronophthisis

American Journal of Kidney Diseases

Volumn 37, Issue 6, 2001, Pages 1131-1139

  Heninger, Erika ^a,b,c   Otto, Edgar ^a,b,c   Imm, Anita ^a,b,c   Caridi, Gianluca ^a,b,c   Hildebrandt, Friedhelm ^a,b,c  

^a UNIVERSITY OF FREIBURG   (Germany)

^b SEMMELWEIS UNIVERSITY   (Hungary)

^c G GASLINI INSTITUTE   (Italy)

Author keywords

Molecular genetic diagnosis; Nephronophthisis; Nephronophthisis type 1 (NPH1); NPHP1

Indexed keywords

ALGORITHM; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; GENE DELETION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; KIDNEY POLYCYSTIC DISEASE; MOLECULAR GENETICS; NEPHRONOPHTHISIS; POINT MUTATION; POLYMERASE CHAIN REACTION;

EID: 0035004046     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1053/ajkd.2001.24514     Document Type: Article

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