A novel SLC6A8 mutation associated with motor dysfunction in a child exhibiting creatine transporter deficiency

  1. Cervera-Acedo, C.
  2. Lopez, M.
  3. Aguirre-Lamban, J.
  4. Santibañez, P.
  5. Garcia-Oguiza, A.
  6. Poch-Olive, M.L.
  7. Dominguez-Garrido, E.
Journal:
Human Genome Variation

ISSN: 2054-345X

Year of publication: 2015

Volume: 2

Issue: 1

Type: Article

DOI: 10.1038/HGV.2015.37 GOOGLE SCHOLAR lock_openOpen access editor

Sustainable development goals

Data source: Scopus