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Research on the genetic and pathologic processes leading to kidney polycystic disease, characterized by the formation of cysts in the renal tubules from epithelial cells. Two main types: autosomal dominant (ADPKD) and autosomal recessive (ARPKD)

#buyrakpolikistozi#gudpaschersindromi#alportsindromi

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Doctor Streange
Doctor StreangeTasdiqlangan muallif
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