A Novel De Novo Mutation of the TITF1/NKX2-1 Gene Causing Ataxia, Benign Hereditary Chorea, Hypothyroidism and a Pituitary Mass in a UK Family and Review of the Literature
Crossref DOI link: https://doi.org/10.1007/s12311-014-0570-7
Published Online: 2014-06-15
Published Print: 2014-10
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Veneziano, Liana
Parkinson, Michael H.
Mantuano, Elide
Frontali, Marina
Bhatia, Kailash P.
Giunti, Paola
License valid from 2014-06-15