학술논문

Heterozygous UCHL1loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy
Document Type
Article
Author
Park, JoohyunTucci, AriannaCipriani, ValentinaDemidov, GermanRocca, ClarissaSenderek, JanButryn, MichaelaVelic, AnaLam, TanyaGalanaki, EvangeliaCali, ElisaVestito, LetiziaMaroofian, RezaDeininger, NatalieRautenberg, MarenAdmard, JakobHahn, Gesa-AstridBartels, Claudiusvan Os, Nienke J.H.Horvath, RitaChinnery, Patrick F.Tiet, May YungHewamadduma, ChannaHadjivassiliou, MariosTofaris, George K.Ambrose, J.C.Arumugam, P.Baple, E.L.Bleda, M.Boardman-Pretty, F.Boissiere, J.M.Boustred, C.R.Brittain, H.Caulfield, M.J.Chan, G.C.Craig, C.E.H.Daugherty, L.C.de Burca, A.Devereau, A.Elgar, G.Foulger, R.E.Fowler, T.Furió-Tarí, P.Hackett, J.M.Halai, D.Hamblin, A.Henderson, S.Holman, J.E.Hubbard, T.J.P.Ibáñez, K.Jackson, R.Jones, L.J.Kasperaviciute, D.Kayikci, M.Lahnstein, L.Lawson, K.Leigh, S.E.A.Leong, I.U.S.Lopez, F.J.Maleady-Crowe, F.Mason, J.McDonagh, E.M.Moutsianas, L.Mueller, M.Murugaesu, N.Need, A.C.Odhams, C.A.Patch, C.Perez-Gil, D.Polychronopoulos, D.Pullinger, J.Rahim, T.Rendon, A.Riesgo-Ferreiro, P.Rogers, T.Ryten, M.Savage, K.Sawant, K.Scott, R.H.Siddiq, A.Sieghart, A.Smedley, D.Smith, K.R.Sosinsky, A.Spooner, W.Stevens, H.E.Stuckey, A.Sultana, R.Thomas, E.R.A.Thompson, S.R.Tregidgo, C.Tucci, A.Walsh, E.Watters, S.A.Welland, M.J.Williams, E.Witkowska, K.Wood, S.M.Zarowiecki, M.Wood, Nicholas W.Hayer, Stefanie N.Bender, FriedemannMenden, BenitaCordts, IsabellKlein, KatrinNguyen, Huu PhucKrauss, Joachim K.Blahak, ChristianStrom, Tim M.Sturm, Marcvan de Warrenburg, BartLerche, HolgerMaček, BorisSynofzik, MatthisOssowski, StephanTimmann, DagmarWolf, Marc E.Smedley, DamianRiess, OlafSchöls, LudgerHoulden, HenryHaack, Tobias B.Hengel, Holger
Source
Genetics in Medicine; October 2022, Vol. 24 Issue: 10 p2079-2090, 12p
Subject
Language
ISSN
10983600; 15300366
Abstract
Biallelic variants in UCHL1have been associated with a progressive early-onset neurodegenerative disorder, autosomal recessive spastic paraplegia type 79. In this study, we investigated heterozygous UCHL1variants on the basis of results from cohort-based burden analyses.