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Rare heterozygous truncating variations and risk of autism spectrum disorder: Whole‐exome sequencing of a multiplex family and follow‐up study in a Japanese population |
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| Authors: | Jun Egawa MD PhD Atsunori Sugimoto MD Ayako Nunokawa MD PhD Masako Shibuya MD PhD Hirofumi Igeta MD Toshiyuki Someya MD PhD |
| Affiliation: | 1. Department of Psychiatry, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan;2. Department of Pediatric Psychiatry, Center for Transdisciplinary Research, Niigata University, Niigata, Japan;3. Oojima Hospital, Niigata, Japan;4. Health Administration Center, Headquarters for Health Administration, Niigata University, Niigata, Japan |
| Abstract: | |
| Keywords: | autism spectrum disorder Japanese multiplex family truncating variation whole‐exome sequencing |