Δευτέρα 20 Νοεμβρίου 2017

SLC52A2 mutations cause SCABD2 phenotype: A second report

Autosomal recessive cerebellar ataxias (ARCAs) are a large group of neurodegenerative disorders that manifest mainly in children and young adults. Most ARCAs are heterogeneous with respect to age at onset, severity of disease progression, and frequency of extracerebellar and systemic signs.

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