Homo sapiens dystrophin (DMD), transcript variant Dp116, mRNA

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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.
Quantitative ultrasonography reveals skeletal muscle abnormalities in carriers of DMD pathogenic variants. [Muscle Nerve. 2024]
Quantitative ultrasonography reveals skeletal muscle abnormalities in carriers of DMD pathogenic variants.
Loureiro BMC, de Brito MR, Iwabe C, Dertkigil SSJ, França MC Jr. Muscle Nerve. 2024 Jun; 69(6):682-690. Epub 2024 Mar 22.

RefSeq alternative splicing
See 44 reference mRNA sequence splice variants for the DMD gene.
RefSeq protein product
See the reference protein sequence for dystrophin isoform Dp116 (NP_004005.2).

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Nucleotide