Publications by authors named "Celine Ledeuil"

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[Genotype-phenotype correlations of pathogenic variants in the FLNC gene].
Flavie Ader, Eric Villard, Céline Ledeuil, Philippe Charron, Pascale Richard

Med Sci (Paris)· November 2018

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Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic Correlations.
Bita Bozorgmehr, Ariana Kariminejad, Shahriar Nafissi, Bita Jebelli, Urtizberea Andoni, Celine Ledeuil

Iran J Child Neurol· March 2014

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Early onset collagen VI myopathies: Genetic and clinical correlations.
Laura Briñas, Pascale Richard, Susana Quijano-Roy, Corine Gartioux, Céline Ledeuil

Ann Neurol· October 2010

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A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy.
Valérie Allamand, Pascale Richard, Alain Lescure, Céline Ledeuil, Delphine Desjardin

EMBO Rep· April 2006

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Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers.
Mariz Vainzof, Pascale Richard, Ralf Herrmann, Cecilia Jimenez-Mallebrera, Beril Talim, Céline Ledeuil

Neuromuscul Disord· October 2005

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Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
Pascale Richard, Philippe Charron, Lucie Carrier, Céline Ledeuil, Theary Cheav

Circulation· May 2003

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