Open AccessInherited renal tubular dysgenesis with novel homozygous mutation in angiotensin-1-converting enzyme gene: A case report
Author(s) -
Michal Kalman,
Tatiana Burjanivová,
Gabriel Minárik,
Veronika Holubeková,
L Plank
Publication year - 2015
Publication title -
case reports in clinical pathology
Language(s) - English
Resource type - Journals
eISSN - 2331-2734
pISSN - 2331-2726
DOI - 10.5430/crcp.v3n1p39
Subject(s) - medicine , oligohydramnios , prenatal diagnosis , anuria , asymptomatic , mutation , dysgenesis , intensive care , pediatrics , fetus , pregnancy , pathology , gene , genetics , intensive care medicine , biology , anatomy