HINT1 Mutations Cause Neuromyotonia in Greek Patients with CMT
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HINT1 Mutations Cause Neuromyotonia in Greek Patients with CMT

According to Charcot-Marie-Tooth News, researchers have associated HINT1 gene mutations with neuropathy in Greek patients with Charcot-Marie-Tooth disease (CMT). In the past, HINT1 was linked to CMT in central and southeastern Europe. However, researchers…

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Could Gene Editing Help with Bainbridge-Ropers Syndrome and Other Rare Diseases?
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Could Gene Editing Help with Bainbridge-Ropers Syndrome and Other Rare Diseases?

It doesn’t seem possible to have a conversation these days without it devolving into some sort of partisan shouting match will little hope of resolution. Issues that we might think…

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