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Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy”

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Published in 2018 at "Neuropsychiatric Disease and Treatment"

DOI: 10.2147/ndt.s179068

Abstract: and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove… read more here.

Keywords: neuropsychiatric disease; response paper; identification novel; titled identification ... See more keywords