Parkinsonism Relat Disord. 2018 Sep 26
Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred.
by
Sveinsson O, Udd B, Svenningsson P, Gassner C, Engström C, Laffita-Mesa JM, Solders G, Hertegård S, Savitcheva I, Jung HH, Tolnay M, Frey BM, Paucar M.