Cite
HARVARD Citation
Kocoglu, C. et al. (2018). Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. Neurology. p. . [Online].
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Kocoglu, C. et al. (2018). Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. Neurology. p. . [Online].