Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
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info:eu-repo/semantics/openAccessDate
2018Author
Kocoglu, CemileGundogdu, Asli
Kocaman, Gulsen
Kahraman-Koytak, Pinar
Uluc, Kayihan
Kiziltan, Gunes
Basak, A. Nazli
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