A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome

  1. Rivera, H.
  2. Martín-Hernández, E.
  3. Delmiro, A.
  4. García-Silva, M.T.
  5. Quijada-Fraile, P.
  6. Muley, R.
  7. Arenas, J.
  8. Martín, M.A.
  9. Martínez-Azorín, F.
Journal:
BMC Nephrology

ISSN: 1471-2369

Year of publication: 2013

Volume: 14

Issue: 1

Type: Article

DOI: 10.1186/1471-2369-14-195 GOOGLE SCHOLAR lock_openOpen access editor

Sustainable development goals

Data source: Scopus