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PubMed for id: 1186517982

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Page 1
A novel homozygous KY variant causing a complex neurological disorder.
Arif B, Rasheed A, Kumar KR, Fatima A, Abbas G, Wohler E, Sobriera N, Lohmann K, Naz S; Baylor-Hopkins Center for Mendelian Genomics. Arif B, et al. Eur J Med Genet. 2020 Nov;63(11):104031. doi: 10.1016/j.ejmg.2020.104031. Epub 2020 Aug 18. Eur J Med Genet. 2020. PMID: 32818658 Free PMC article.
Progressive hereditary spastic paraplegia caused by a homozygous KY mutation.
Yogev Y, Perez Y, Noyman I, Madegem AA, Flusser H, Shorer Z, Cohen E, Kachko L, Michaelovsky A, Birk R, Koifman A, Drabkin M, Wormser O, Halperin D, Kadir R, Birk OS. Yogev Y, et al. Eur J Hum Genet. 2017 Aug;25(8):966-972. doi: 10.1038/ejhg.2017.85. Epub 2017 May 10. Eur J Hum Genet. 2017. PMID: 28488683 Free PMC article.
Human gingiva transcriptome during wound healing.
Wang Y, Tatakis DN. Wang Y, et al. J Clin Periodontol. 2017 Apr;44(4):394-402. doi: 10.1111/jcpe.12669. Epub 2017 Feb 11. J Clin Periodontol. 2017. PMID: 28005267