[1]
Tavian, D., Durdu, M., Angelini, C., Torre, E. and Missaglia, S. 2021. Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome. European Journal of Translational Myology. 31, 2 (May 2021). DOI:https://doi.org/10.4081/ejtm.2021.9796.