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


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

NEUROLOGY-GENETICS, vol.4, no.1, 2018 (SCI-Expanded, Scopus) identifier identifier identifier