Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry

Sanson B, Slioui A, Garcia J, Klouvi L, Lejeune J, Stalens C, Guien C, Rabarimeriarijaona S, Bernard R, Nectoux J, Attarian S, Bedat-Millet AL, Bouhour F, Boyer FC, Chanson JB, Choumert A, Cintas P, De La Cruz E, Féasson L, Fournier M, Ghorab K, Jacquin-Piques A, Laforet P, Magot A, Michaud M, Noury JB, Sole G, Spinazzi M, Stojkovic T, Tard C, Villa L, Beroud C, Sacconi S

Orphanet journal of rare diseases