Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families


Kocoglu C., Gundogdu A., Kocaman G., KAHRAMAN KOYTAK P. , ULUÇ K. , KIZILTAN G., ...More

NEUROLOGY-GENETICS, vol.4, no.1, 2018 (Journal Indexed in ESCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 4 Issue: 1
  • Publication Date: 2018
  • Doi Number: 10.1212/nxg.0000000000000218
  • Title of Journal : NEUROLOGY-GENETICS