At the DNM1L Foundation, we often hear a big question from families:
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DNM1L genetic variations, though rare, have a profound impact on those affected, influencing everything from motor skills ...
DNM1L is a rare genetic disorder that affects mitochondrial function, leading to severe developmental delays, neurological issues, ...
DNM1L is a rare genetic disorder that disrupts mitochondrial function, leading to a range of severe symptoms ...
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