Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes.
Hui WangTimothy S ChangBeth A DombroskiPo-Liang ChengYa-Qin SiAlbert TucciVishakha PatilLeopoldo Valiente-BanuetKurt FarrellCatriona McleanLaura Molina-PorcelRajput AlexPeter Paul de DeynNathalie Le BastardMarla GearingLaura Donker KaatJohn C Van SwietenElise DopperBernardino F GhettiKathy L NewellClaire TroakesJusto G de YébenesAlberto Rábano-GutierrezTina MellerWolfgang Hermann OertelGesine RespondekMaria StamelouThomas ArzbergerSigrun RoeberUlrich MüllerFranziska HopfnerPau PastorAlexis BriceAlexandra DurrIsabelle Le BerThomas G BeachGeidy E SerranoLili-Naz HazratiIrene LitvanRosa RademakersOwen A RossDouglas GalaskoAdam L BoxerBruce L MillerWillian W SeeleyVivanna M Van DeerlinEdward B LeeCharles L WhiteHuw R MorrisRohan de SilvaJohn F CraryAlison Mary GoateJeffrey S FriedmanYuk Yee LeungGiovanni CoppolaAdam C NajLi-San Wangnull nullDennis W DicksonGünter U HöglingerJung-Ying TzengDaniel H GeschwindGerard D SchellenbergWan-Ping LeePublished in: medRxiv : the preprint server for health sciences (2024)
The association between the H1 and H2 haplotypes and PSP involves multiple contributing factors, including the copy number of γ duplication.