Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's disease.
Parkinsonism & Related Disorders
Soto-Beasley, Alexandra I AI; Walton, Ronald L RL; Valentino, Rebecca R RR; Hook, Paul W PW; Labbé, Catherine C; Heckman, Michael G MG; Johnson, Patrick W PW; Goff, Loyal A LA; Uitti, Ryan J RJ; McLean, Pamela J PJ; Springer, Wolfdieter W; McCallion, Andrew S AS; Wszolek, Zbigniew K ZK; Ross, Owen A OA
Publication Date: 2020-09
Variant appearance in text: KANSL1: P712P; rs2277613
Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S
A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.
Deleterious coding variants in multi-case families with non-syndromic cleft lip and/or palate phenotypes.
Scientific Reports
Pengelly, Reuben J RJ; Arias, Liliana L; Martínez, Julio J; Upstill-Goddard, Rosanna R; Seaby, Eleanor G EG; Gibson, Jane J; Ennis, Sarah S; Collins, Andrew A; Briceño, Ignacio I
Publication Date: 2016-07-26
Variant appearance in text: KANSL1: P712P; rs2277613
Whole-genome sequencing of the world's oldest people.
Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014
Variant appearance in text: KANSL1: P712P; rs2277613