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

Title:	Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry
Authors:	Sanson, Benoît^{Aff1, IDs1302302503877z_cor1}; Slioui, Abderhmane^{Aff1, Aff2}; Garcia, Jérémy^Aff1; Klouvi, Lori^Aff3; Lejeune, Julie^Aff3; Stalens, Caroline^Aff3; Guien, Céline^Aff4; Rabarimeriarijaona, Sitraka^Aff5; Bernard, Rafaëlle^Aff5; Nectoux, Juliette^Aff6; Attarian, Sharham^Aff7; Bédat-Millet, Anne-Laure^Aff8; Bouhour, Françoise^Aff9; Boyer, François Constant^Aff10; Chanson, Jean-Baptiste^Aff11; Choumert, Ariane^Aff12; Cintas, Pascal^Aff13; De La Cruz, Elisa^Aff14; Féasson, Léonard^Aff15; Fournier, Maxime^Aff16; Ghorab, Karima^Aff17; Jacquin-Piques, Agnès^Aff18; Laforêt, Pascal^Aff19; Magot, Armelle^Aff20; Michaud, Maud^Aff21; Noury, Jean-Baptiste^Aff22; Solé, Guilhem^Aff23; Spinazzi, Marco^Aff24; Stojkovic, Tanya^Aff25; Tard, Céline^Aff26; Villa, Luisa^Aff1; Béroud, Christophe^{Aff5, Aff27}; Sacconi, Sabrina^{Aff1, Aff28}
Source:	Orphanet Journal of Rare Diseases. 20(1)
Database:	Springer Nature Journals