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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 2 |
2022 | 1 |
2024 | 1 |
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Page 1
Heterozygous De Novo Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar Localization.
Genes (Basel). 2021 Dec 24;13(1):51. doi: 10.3390/genes13010051.
Genes (Basel). 2021.
PMID: 35052391
Free PMC article.
Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder.
Khan H, Harripaul R, Mikhailov A, Herzi S, Bowers S, Ayub M, Shabbir MI, Vincent JB.
Khan H, et al.
Sci Rep. 2024 Apr 22;14(1):9230. doi: 10.1038/s41598-024-57942-x.
Sci Rep. 2024.
PMID: 38649688
Free PMC article.
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Biallelic Loss of Function Mutation in Sodium Channel Gene SCN10A in an Autism Spectrum Disorder Trio from Pakistan.
Rabia A, Harripaul R, Mikhailov A, Mahmood S, Maqbool S, Vincent JB, Ayub M.
Rabia A, et al.
Genes (Basel). 2022 Sep 11;13(9):1633. doi: 10.3390/genes13091633.
Genes (Basel). 2022.
PMID: 36140801
Free PMC article.
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Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14.
Pastore SF, Muhammad T, Harripaul R, Lau R, Khan MTM, Khan MI, Islam O, Kang C, Ayub M, Jelani M, Vincent JB.
Pastore SF, et al.
Sci Rep. 2021 Nov 30;11(1):23113. doi: 10.1038/s41598-021-02599-z.
Sci Rep. 2021.
PMID: 34848785
Free PMC article.
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