A. Lunati

The genetic landscape of Parkinson's disease.

A. Brice, S. Lesage, A. Lunati, 2018, Revue neurologique.

Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation

G. Bouyer, L. Garçon, L. Kiger, 2021, American journal of hematology.

VPS4A mutation in syndromic congenital hemolytic anemia without obvious signs of dyserythropoiesis

C. Garel, B. Funalot, F. Galactéros, 2021, American journal of hematology.

Characterization of Recessive Parkinson Disease in a Large Multicenter Study

A. Singleton, M. Vidailhet, F. Viallet, 2020, Annals of neurology.

Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants

A. Toutain, P. Calvas, B. Gilbert-Dussardier, 2019, Journal of the Neurological Sciences.

Comparison of cardiac involvement, extracardiac manifestations and outcomes between homozygote and heterozygote transthyretin p.Val142Ile (V122I) variant in patients with hereditary transthyretin amyloidosis: a cohort study

E. Teiger, L. Hittinger, B. Funalot, 2023, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.