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	1.	A novel mutation (delAACT) in the tyrosinase gene in a Cameroonian black with type 1A oculocutaneous albinism. [electronic resource] by Badens, Catherine Courrier, Sébastien Aquaron, Robert Producer: 20060622 In: Journal of dermatological science vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Dysferlin Exon 32 Skipping in Patient Cells. [electronic resource] by Barthélémy, Florian Courrier, Sébastien Lévy, Nicolas Krahn, Martin Bartoli, Marc Producer: 20190401 In: Methods in molecular biology (Clifton, N.J.) vol. 1828 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	ATRX syndrome in a girl with a heterozygous mutation in the ATRX Zn finger domain and a totally skewed X-inactivation pattern. [electronic resource] by Badens, Catherine Martini, Nathalie Courrier, Sébastien DesPortes, Vincent Touraine, Renaud Levy, Nicolas Edery, Patrick Producer: 20061213 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Comparing targeted exome and whole exome approaches for genetic diagnosis of neuromuscular disorders. [electronic resource] by Gorokhova, Svetlana Cerino, Mathieu Mathieu, Yves Courrier, Sébastien Desvignes, Jean-Pierre Salgado, David Béroud, Christophe Krahn, Martin Bartoli, Marc Producer: 20160407 In: Applied & translational genomics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Further heterogeneity in myopathy with tubular aggregates? [electronic resource] by De Paula, Andre Maues Bartoli, Marc Courrier, Sebastien Pouget, Jean Levy, Nicolas Pellissier, Jean-François Figarella-Branger, Dominique Krahn, Martin Attarian, Shahram Producer: 20130211 In: Muscle & nerve vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Ectomycorrhizal symbiosis affects functional diversity of rhizosphere fluorescent pseudomonads. [electronic resource] by Frey-Klett, Pascale Chavatte, Michaël Clausse, Marie-Lise Courrier, Sébastien Le Roux, Christine Raaijmakers, Jos Martinotti, Maria Giovanna Pierrat, Jean-Claude Garbaye, Jean Producer: 20050531 In: The New phytologist vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Exon 32 Skipping of Dysferlin Rescues Membrane Repair in Patients' Cells. [electronic resource] by Barthélémy, Florian Blouin, Cédric Wein, Nicolas Mouly, Vincent Courrier, Sébastien Dionnet, Eugénie Kergourlay, Virginie Mathieu, Yves Garcia, Luis Butler-Browne, Gillian Lamaze, Christophe Lévy, Nicolas Krahn, Martin Bartoli, Marc Publication details: Journal of neuromuscular diseases Sep 2015 In: Journal of neuromuscular diseases vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	High prevalence of laminopathies among patients with metabolic syndrome. [electronic resource] by Dutour, Anne Roll, Patrice Gaborit, Bénédicte Courrier, Sébastien Alessi, Marie-Christine Tregouet, David-Alexandre Angelis, Fabien Robaglia-Schlupp, Andrée Lesavre, Nathalie Cau, Pierre Lévy, Nicolas Badens, Catherine Morange, Pierre-Emmanuel Producer: 20120120 In: Human molecular genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A naturally occurring human minidysferlin protein repairs sarcolemmal lesions in a mouse model of dysferlinopathy. [electronic resource] by Krahn, Martin Wein, Nicolas Bartoli, Marc Lostal, William Courrier, Sébastien Bourg-Alibert, Nathalie Nguyen, Karine Vial, Christophe Streichenberger, Nathalie Labelle, Véronique DePetris, Danielle Pécheux, Christophe Leturcq, France Cau, Pierre Richard, Isabelle Lévy, Nicolas Producer: 20110120 In: Science translational medicine vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors. [electronic resource] by Navarro, Claire L Cadiñanos, Juan De Sandre-Giovannoli, Annachiara Bernard, Rafaëlle Courrier, Sébastien Boccaccio, Irène Boyer, Amandine Kleijer, Wim J Wagner, Anja Giuliano, Fabienne Beemer, Frits A Freije, Jose M Cau, Pierre Hennekam, Raoul C M López-Otín, Carlos Badens, Catherine Lévy, Nicolas Producer: 20051128 In: Human molecular genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update. [electronic resource] by Navarro, Claire Laure Esteves-Vieira, Vera Courrier, Sébastien Boyer, Amandine Duong Nguyen, Thuy Huong, Le Thi Thanh Meinke, Peter Schröder, Winnie Cormier-Daire, Valérie Sznajer, Yves Amor, David J Lagerstedt, Kristina Biervliet, Martine van den Akker, Peter C Cau, Pierre Roll, Patrice Lévy, Nicolas Badens, Catherine Wehnert, Manfred De Sandre-Giovannoli, Annachiara Producer: 20150330 In: European journal of human genetics : EJHG vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)