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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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An AOA2 patient with a novel compound heterozygous SETX frame shift mutations
Emi Motokura1, Toru Yamashita1, Yoshiaki Takahashi1
1Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, 2-5-1 Shikatacho, Okayama 700-8558, Japan.
Journal of the Neurological Sciences
|December 27, 2016
Summary
No abstract available in PubMed .
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