Renal-retinal syndromes: Association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus

American Journal of Kidney Diseases

Volumn 32, Issue 6, 1998, Pages 1059-1062

  Caridi, G ^a   Murer, L ^a   Bellantuono, R ^a   Sorino, P ^a   Caringella, D A ^a   Gusmano, R ^a   Ghiggeri, G M ^a  

^a G GASLINI INSTITUTE   (Italy)

Author keywords

Nephronophthisis; NPH1 gene locus; Retinal dystrophy

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 2Q; CLINICAL ARTICLE; DISEASE ASSOCIATION; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MOLECULAR GENETICS; NEPHRONOPHTHISIS; PRESCHOOL CHILD; RENAL RETINAL SYNDROME; RETINA MALFORMATION; SYNDROME DELINEATION;

EID: 0031742106     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0272-6386(98)70083-6     Document Type: Article

References (12)