Linkage analysis and exome sequencing identify a novel mutation inKCTD7in patients with progressive myoclonus epilepsy with ataxia-Reference-Cited by-同舟云学术

Linkage analysis and exome sequencing identify a novel mutation inKCTD7in patients with progressive myoclonus epilepsy with ataxia

Author:

Farhan Sali M. K.¹²,Murphy Lisa M.¹,Robinson John F.¹,Wang Jian¹,Siu Victoria M.²³⁴,Rupar C. Anthony²³⁴,Prasad Asuri N.⁴⁵,Hegele Robert A.¹²,

Affiliation:

1. Robarts Research Institute; Schulich School of Medicine and Dentistry; Western University; London Ontario Canada

2. Department of Biochemistry; Schulich School of Medicine and Dentistry; Western University; London Ontario Canada

3. Medical Genetics Program; Department of Pediatrics; London Health Sciences Centre; London Ontario Canada

4. Children's Health Research Institute; London Health Sciences Centre; London Ontario Canada

5. Division of Clinical Neurological Sciences; Department of Pediatrics; London Health Sciences Centre; London Ontario Canada

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

Reference12 articles.

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