Similar articles

• Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule.

  Aartsma-Rus A, Van Deutekom JC, Fokkema IF, Van Ommen GJ, Den Dunnen JT. Aartsma-Rus A, et al. Muscle Nerve. 2006 Aug;34(2):135-44. doi: 10.1002/mus.20586. Muscle Nerve. 2006. PMID: 16770791 Review.
• Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.

  Tuffery-Giraud S, Béroud C, Leturcq F, Yaou RB, Hamroun D, Michel-Calemard L, Moizard MP, Bernard R, Cossée M, Boisseau P, Blayau M, Creveaux I, Guiochon-Mantel A, de Martinville B, Philippe C, Monnier N, Bieth E, Khau Van Kien P, Desmet FO, Humbertclaude V, Kaplan JC, Chelly J, Claustres M. Tuffery-Giraud S, et al. Hum Mutat. 2009 Jun;30(6):934-45. doi: 10.1002/humu.20976. Hum Mutat. 2009. PMID: 19367636
• Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations.

  Aartsma-Rus A, Fokkema I, Verschuuren J, Ginjaar I, van Deutekom J, van Ommen GJ, den Dunnen JT. Aartsma-Rus A, et al. Hum Mutat. 2009 Mar;30(3):293-9. doi: 10.1002/humu.20918. Hum Mutat. 2009. PMID: 19156838 Review.
• Novel human pathological mutations. Gene symbol: DMD. Disease: muscular dystrophy, Duchenne.

  Garcia-Planells J, Torres-Puente M, Vilchez JJ, Pérez-Alonso M. Garcia-Planells J, et al. Hum Genet. 2009 Aug;126(2):338. Hum Genet. 2009. PMID: 19694016 No abstract available.
• Novel human pathological mutations. Gene symbol: DMD. Disease: muscular dystrophy, Duchenne.

  Garcia-Planells J, Torres-Puente M, Vilchez JJ, Perez-Alonso M. Garcia-Planells J, et al. Hum Genet. 2009 Aug;126(2):338. Hum Genet. 2009. PMID: 19694014 No abstract available.