J. Graafland

Paroxysmal exercise‐induced dystonia within the phenotypic spectrum of ECHS1 deficiency

W. Mandemakers, R. Jech, E. Barbosa, 2016, Movement disorders : official journal of the Movement Disorder Society.

The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.

M. Emre, M. Gultekin, A. Yalcin, 2017, Parkinsonism & related disorders.

An exome study of Parkinson’s disease in Sardinia, a Mediterranean genetic isolate

E. Tolosa, F. Valldeoriola, C. Mariani, 2014, neurogenetics.

DNAJC6 Mutations Associated With Early‐Onset Parkinson's Disease

W. Mandemakers, Jun Wang, Jianguo Zhang, 2016, Annals of neurology.

Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early‐Onset Parkinsonism

S. Pappatà, Jun Wang, P. Barone, 2013, Human mutation.

Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes

G. Breedveld, V. Bonifati, M. Quadri, 2015, Movement disorders : official journal of the Movement Disorder Society.

Early-onset parkinsonism caused by alpha-synuclein gene triplication: Clinical and genetic findings in a novel family.

Vincenzo Bonifati, Astrid Thomas, Marco Onofrj, 2015, Parkinsonism & related disorders.