Whole‐exome sequencing reveals a missense mutation in the KCND3 gene in a patient with SCA19/22

Publisher: John Wiley & Sons Inc

E-ISSN: 2049-4173|3|5|197-199

ISSN: 2049-4173

Source: Neurology And Clinical Neuroscience (Electronic), Vol.3, Iss.5, 2015-09, pp. : 197-199

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Abstract