disease 1,684 words KG: ent-dise-c4dab5af
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Becker Muscular Dystrophy

Disease Info
In-frame deletionsRemoval of one or more exons that maintain the reading frame, allowing production of a truncated but partially functional protein. These account for approximately 65-70% of BMD cases.
In-frame duplicationsAdditional copies of exons that also preserve the reading frame.
Missense mutationsAmino acid substitutions that partially impair dystrophin function without abolishing it.
Reduced dystrophin levelsTypically 10-30% of normal
Truncated proteinOften missing internal segments
Partially preserved functionCan still provide some membrane protection
DatabasesOMIMOrphanetClinicalTrialsPubMed

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