The Alu insertion in the CLCN5 gene of a patient with Dent's disease leads to exon 11 skipping

  1. Claverie-Martín, F.
  2. Flores, C.
  3. Antón-Gamero, M.
  4. González-Acosta, H.
  5. García-Nieto, V.
Journal:
Journal of Human Genetics

ISSN: 1434-5161

Year of publication: 2005

Volume: 50

Issue: 7

Pages: 370-374

Type: Article

DOI: 10.1007/S10038-005-0265-5 GOOGLE SCHOLAR lock_openOpen access editor
Data source: Scopus