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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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RALA mutation in a patient with autism spectrum disorder and Noonan syndrome-like phenotype
Nobuhiko Okamoto1,2, Atsushi Takata3, Noriko Miyake3
1Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan.
Congenital Anomalies
|February 15, 2019
Abstract
No abstract available in PubMed .
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