INHERITED PATHOLOGY OF β2-LAMININ (PIERSON SYNDROME): CLINICAL AND GENETIC ASPECTS
For the last decade a great successes were attained in the study of molecular bases of glomerular diseases. It was certain that the most frequent reasons of congenital and infantile nephrotic syndrome are mutations in the genes of NPHS1, NPHS2, and WT1. Nevertheless, until now, a number of patients,...
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Union of pediatricians of Russia,
2010-05-01T00:00:00Z.
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