Kelly Regan-Fendt
1PUBLICATIONS
7CO-AUTHORS

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Publications (1)
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|Dec 04, 2025
Long-Read Genome Sequencing Establishes Biallelic Pathogenic Variants in DNM1 With Distinct Functional Effects as the Cause of Early Infantile Developmental and Epileptic Encephalopathy.Andy Drackley, Merlene Peter, Heba H Akbari
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