Publication | Open Access

Identification of Constitutional WT1 Mutations, in Patients with Isolated Diffuse Mesangial Sclerosis, and Analysis of Genotype/Phenotype Correlations by Use of a Computerized Mutation Database

SclerodermaGenetic DisorderMedicineGeneticsGenetic EpidemiologyDiagnosisPathologyConstitutional Wt1 MutationsComputerized Mutation DatabaseBiostatisticsGenotype/phenotype CorrelationsDisease Gene IdentificationMonogenic DisordersNeuropathologyMolecular DiagnosticsPublic HealthTuberous SclerosisClinical Genetics