T. Conte

BAG3P215L/KO mice as a model of BAG3P209L myofibrillar myopathy.

Jason C. Young, A. Sadikot, R. Bryson-Richardson, 2020, The American journal of pathology.

Sacs knockout mice present pathophysiological defects underlying autosomal recessive spastic ataxia of Charlevoix-Saguenay.

E. Shoubridge, B. Brais, P. McPherson, 2015, Human molecular genetics.

Diagnostic anoctamin‐5 protein defect in patients with ANO5‐mutated muscular dystrophy

B. Brais, I. Richard, B. Eymard, 2018, Neuropathology and applied neurobiology.