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Parkinsonism Relat Disord. 2018 Sep 26

Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred.

by Christoph Gassner

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.

PMID: Parkinsonism Relat Disord. 2018 Sep 26. pii: S1353-8020(18)30399-7. doi: 10.1016/j.parkreldis.2018.09.014. [Epub ahead of print]

↗ https://www.ncbi.nlm.nih.gov/pubmed