Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16.

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Prior TW, Bartolo C, Papp AC, Snyder PJ, Sedra MS, Burghes AH, Mendell JR

Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16.

Hum Mol Genet. 1994 Jul;3(7):1173-4. doi: 10.1093/hmg/3.7.1173.

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7981690 [ View in PubMed
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DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
DystrophinP11532Details