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, Bédat-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, Laforêt P, Magot A, Michaud M, Noury JB, Solé G, Spinazzi M, Stojkovic T, Tard C, Villa L, Béroud C, Sacconi S; French FSHD registry collaboration group.
Sanson B, et al. Among authors: ghorab k.
Orphanet J Rare Dis. 2025 Sep 2;20(1):470. doi: 10.1186/s13023-025-03877-z.
Orphanet J Rare Dis. 2025.
PMID: 40898356
Free PMC article.