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- W4290974983 abstract "O gene DMD localiza-se no cromossomo X e codifica a distrofina, uma proteína do citoesqueleto responsável pela manutenção da integridade e da função contrátil das fibras musculares. Alterações moleculares no gene DMD interferem na produção da distrofina, resultando no desenvolvimento de uma doença degenerativa conhecida como Distrofia Muscular de Duchenne (DMD). A DMD é uma doença de herança recessiva ligada ao cromossomo X, causada por mutações, principalmente deleçõesno gene DMD. A doença acomete, em sua maioria, homens e caracteriza-se por fraqueza muscular progressiva detectada nos primeiros anos de vida." @default.
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- W4290974983 date "2020-05-24" @default.
- W4290974983 modified "2023-10-05" @default.
- W4290974983 title "Gene DMD e a distrofia muscular de Duchenne" @default.
- W4290974983 doi "https://doi.org/10.55838/1980-3540.ge.2020.345" @default.
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