| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5680842 | Medicina Clínica | 2017 | 5 Pages |
Abstract
The presence of FSGS or other kidney involvement accompanied by hereditary neurosensory deafness and T2DM could be suggestive of a A3243G tRNALeu mutation and should prompt a genetic testing and an evaluation of potential extrarenal involvement.
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Authors
Pau Alcubilla-Prats, Manel Solé, Albert Botey, Josep Maria Grau, Glòria Garrabou, Esteban Poch,