Homo sapiens partial DMD gene for dystrophin, exons 49-50

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Identifying inversions with breakpoints in the Dystrophin gene through long-read sequencing: report of two cases. [BMC Med Genomics. 2024]
Identifying inversions with breakpoints in the Dystrophin gene through long-read sequencing: report of two cases.
Chen L, Luo X, Wang H, Tian Y, Liu Y. BMC Med Genomics. 2024 Sep 9; 17(1):227. Epub 2024 Sep 9.
Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD gene. [Neuromuscul Disord. 2024]
Long-term clinical follow-up of a family with Becker muscular dystrophy associated with a large deletion in the DMD gene.
Davies KE, Vogt J. Neuromuscul Disord. 2024 Jun; 39:5-9. Epub 2024 Apr 14.
Novel mutation leading to splice donor loss in a conserved site of DMD gene causes Duchenne muscular dystrophy with cryptorchidism. [J Med Genet. 2024]
Novel mutation leading to splice donor loss in a conserved site of DMD gene causes Duchenne muscular dystrophy with cryptorchidism.
Chen J, Jia Y, Zhong J, Zhang K, Dai H, He G, Li F, Zeng L, Fan C, Xu H. J Med Genet. 2024 Jul 19; 61(8):741-749. Epub 2024 Jul 19.

RefSeq alternative splicing
See 44 reference mRNA sequence splice variants for the DMD gene.

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Nucleotide