Focused on myotonic dystrophy type 1. My use of twitter/X is not an endorsement of the ninny who owns it. Follow me on Bluesky, https://xitter.cf/t.co/HrlGRPWgJw

Joined May 2013
If you or a family member have myotonic dystrophy, the #1 thing you can do to help researchers develop an effective treatment is to enroll in the END-DM1 natural history study. Details here: clinicaltrials.gov/ct2/show/…
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ASHG Abstract from Quebec: Leveraging a founder population to identify genetic modifiers of myotonic dystrophy type 1 ashg.floq.live/event/ashg-20…
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ASHG abstract from Quest Diagnostics: Co-occurrence of CLCN1 variants with myotonic dystrophy repeat expansions (DM1/DM2) ashg.floq.live/event/ashg-20…
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$IONS/Quebec/NYU study:
Antisense-mediated gene therapy targeting DMPK restores cardiac ion channel function and electrical stability in myotonic dystrophy type 1 #OpenAccess heartrhythmjournal.com/artic…
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Bunch of abstracts on myotonic dystrophy presented at World Muscle Society Conference Sept. 29-Oct. 3. Can search for full text of abstracts at link below. Will post some of titles in comments. nmd-journal.com/action/doSea…
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