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

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Title: Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry.
Authors: Sanson, Benoît1 (AUTHOR) sanson.b@chu-nice.fr, Slioui, Abderhmane1,2 (AUTHOR), Garcia, Jérémy1 (AUTHOR), Klouvi, Lori3 (AUTHOR), Lejeune, Julie3 (AUTHOR), Stalens, Caroline3 (AUTHOR), Guien, Céline4 (AUTHOR), Rabarimeriarijaona, Sitraka5 (AUTHOR), Bernard, Rafaëlle5 (AUTHOR), Nectoux, Juliette6 (AUTHOR), Attarian, Sharham7 (AUTHOR), Bédat-Millet, Anne-Laure8 (AUTHOR), Bouhour, Françoise9 (AUTHOR), Boyer, François Constant10 (AUTHOR), Chanson, Jean-Baptiste11 (AUTHOR), Choumert, Ariane12 (AUTHOR), Cintas, Pascal13 (AUTHOR), De La Cruz, Elisa14 (AUTHOR), Féasson, Léonard15 (AUTHOR), Fournier, Maxime16 (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 9/2/2025, Vol. 20 Issue 1, p1-12. 12p.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 9/2/2025, Vol. 20 Issue 1, p1-12. 12p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=187699670
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              Text: 9/2/2025
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