Publication | Open Access
Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria
41
Citations
15
References
1997
Year
Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene IdentificationMedicineClcn5 GeneNephrologyJapanese PatientsClinical Genetics
| Year | Citations | |
|---|---|---|
Page 1
Page 1