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
2015 ◽
Vol 69
(8)
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pp. 472-476
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2015 ◽
Vol 229
(1-2)
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pp. 599-601
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Keyword(s):
2019 ◽
Vol 50
(6)
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pp. 2247-2251
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Keyword(s):
2019 ◽
Vol 58
(3)
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pp. 376-377
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Keyword(s):
Keyword(s):
2016 ◽
Vol 26
(6)
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pp. 297-301
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2021 ◽
pp. 1-11
Keyword(s):