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Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype

Title: Rare variation in neurological disease genes and its role in multiple sclerosis mimicry and phenotype
Authors: Blackburn, Nicholas B.Aff1, IDs1307302501582x_cor1; McComish, Bennet J.Aff1; Motyer, AllanAff2, Aff3; Slimmer, James C.Aff1; Leslie, Stephen J.Aff2, Aff3; Broadley, Simon A.Aff4; Jokubaitis, Vilija G.Aff5, Aff6; Van Der Walt, AnnekeAff5, Aff6; Kermode, Allan G.Aff7, Aff8; Lechner-Scott, JeannetteAff9, Aff10, Aff11; Parnell, Grant P.Aff12, Aff13; Fabis-Pedrini, Marzena J.Aff7, Aff8; Scott, Rodney J.Aff14; Jackson, StaceyAff15, Aff16; Maltby, Vicki E.Aff9, Aff10, Aff11; Charlesworth, Jac C.Aff1; Burdon, Kathryn P.Aff1; Taylor, Bruce V.Aff1; Kilpatrick, Trevor J.Aff15, Aff16, Aff17; Rubio, Justin P.Aff15, Aff16, IDs1307302501582x_cor2
Source: Genome Medicine. 17(1)
Database: Springer Nature Journals