A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsy.

Neurol Sci

Neurology Department, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.

Published: January 2021

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http://dx.doi.org/10.1007/s10072-020-04559-3	DOI Listing

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