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	1.	Revised spectrum of mutations in sarcoglycanopathies. [electronic resource] by Trabelsi, Madiha Kavian, Niloufar Daoud, Fatma Commere, Virginie Deburgrave, Nathalie Beugnet, Caroline Llense, Stephane Barbot, Jean Claude Vasson, Aurélie Kaplan, Jean Claude Leturcq, France Chelly, Jamel Producer: 20080916 In: European journal of human genetics : EJHG vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene. [electronic resource] by Deburgrave, Nathalie Daoud, Fatma Llense, Stéphane Barbot, Jean Claude Récan, Dominique Peccate, Cécile Burghes, Arthur H M Béroud, Christophe Garcia, Luis Kaplan, Jean-Claude Chelly, Jamel Leturcq, France Producer: 20070228 In: Human mutation vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene. [electronic resource] by Béroud, Christophe Carrié, Alain Beldjord, Chérif Deburgrave, Nathalie Llense, Stéphane Carelle, Nadège Peccate, Cécile Cuisset, Jean Marie Pandit, Florence Carré-Pigeon, Frédérique Mayer, Michèle Bellance, Rémi Récan, Dominique Chelly, Jamel Kaplan, Jean Claude Leturcq, France Producer: 20040309 In: Neuromuscular disorders : NMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)