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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2015 | 1 |
2018 | 1 |
2021 | 1 |
2024 | 0 |
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Page 1
Excess of rare, inherited truncating mutations in autism.
Nat Genet. 2015 Jun;47(6):582-8. doi: 10.1038/ng.3303. Epub 2015 May 11.
Nat Genet. 2015.
PMID: 25961944
Free PMC article.
A method to delineate de novo missense variants across pathways prioritizes genes linked to autism.
Koire A, Katsonis P, Kim YW, Buchovecky C, Wilson SJ, Lichtarge O.
Koire A, et al.
Sci Transl Med. 2021 May 19;13(594):eabc1739. doi: 10.1126/scitranslmed.abc1739.
Sci Transl Med. 2021.
PMID: 34011629
Free PMC article.
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Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study.
Männikkö R, Wong L, Tester DJ, Thor MG, Sud R, Kullmann DM, Sweeney MG, Leu C, Sisodiya SM, FitzPatrick DR, Evans MJ, Jeffrey IJM, Tfelt-Hansen J, Cohen MC, Fleming PJ, Jaye A, Simpson MA, Ackerman MJ, Hanna MG, Behr ER, Matthews E.
Männikkö R, et al.
Lancet. 2018 Apr 14;391(10129):1483-1492. doi: 10.1016/S0140-6736(18)30021-7. Epub 2018 Apr 5.
Lancet. 2018.
PMID: 29605429
Free PMC article.
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