Publication | Open Access
Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS
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Citations
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References
2008
Year
Genetic AnalysisMendelian DisorderGenetic DisorderMedicineGeneticsGenetic EpidemiologyMolecular GeneticsDisease Gene IdentificationGenomicsPublic HealthSystems BiologyMolecular DiagnosticsHomozygous Plce1Hereditary Fsgs
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