Congenital anomalies of the kidney and urinary tract - Role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene

Journal of Urology

Volumn 165, Issue 1, 2001, Pages 196-202

  Pope IV, John C ^a,b,c   Brock III, John W ^a,b,c   Adams, Mark C ^a,b,c   Miyazaki, Yoichi ^a,b,c   Stephens, F Douglas ^a,b,c   Ichikawa, Iekuni ^a,b,c  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b TOKAI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

Abnormalities; Angiotensin II; Genes; Kidney; Urinary tract

Indexed keywords

ANGIOTENSIN; ANGIOTENSIN 1 RECEPTOR; ANGIOTENSIN 2 RECEPTOR;

ECTOPIC URETER; EMBRYONIC STRUCTURES; GENE DELETION; GENE MUTATION; KIDNEY ANOMALY; KIDNEY DEVELOPMENT; MULTIFACTORIAL INHERITANCE; ONTOGENY; PLEIOTROPY; PRIORITY JOURNAL; RECEPTOR GENE; REVIEW; URINARY TRACT MALFORMATION;

EID: 0034749269     PISSN: 00225347     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005392-200101000-00057     Document Type: Review

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