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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, Allan^{Aff2, Aff3}; Slimmer, James C.^Aff1; Leslie, Stephen J.^{Aff2, Aff3}; Broadley, Simon A.^Aff4; Jokubaitis, Vilija G.^{Aff5, Aff6}; Van Der Walt, Anneke^{Aff5, Aff6}; Kermode, Allan G.^{Aff7, Aff8}; Lechner-Scott, Jeannette^{Aff9, Aff10, Aff11}; Parnell, Grant P.^{Aff12, Aff13}; Fabis-Pedrini, Marzena J.^{Aff7, Aff8}; Scott, Rodney J.^Aff14; Jackson, Stacey^{Aff15, 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