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Dive into the research topics of 'Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnostics'. Together they form a unique fingerprint.- Sort by
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Reza Vazifehmand, Sandro Rossetti, Sassan Saber, Hamid Reza Khorram Khorshid, Peter C. Harris
Research output: Contribution to journal › Article › peer-review