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Fig. 2 | BMC Neurology

Fig. 2

From: Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene

Fig. 2

Displays the Sanger sequencing map of the KCNC3 gene in patients and families. A red circle indicates the mutation site. (A) The patient’s KCNC3 gene (located at chr19:50826942) exhibited a heterozygous variation of c.1268 G > A. (B) A heterozygous mutation of c.1268 G > A achr19:50826942 was also present in the patient’s mother. (C) Fater of the patient did not have any mutations

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BMC Neurology

ISSN: 1471-2377

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