DOI:
10.1055/s-00029025
Journal of Pediatric Epilepsy
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References
Staropoli JF, Karaa A, Lim ET , et al.
A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system.
Am J Hum Genet 2012;
91 (1) 202-208
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