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Parent-of-Origin Effect on the Age at Symptom Onset in Myotonic Dystrophy Type 2.

Neurol Genet · 2023 · PMC10136683 · PMID 37123986

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Although differences did not reach statistical significance, presumed congenital/very early-onset (first decade) symptoms, cataracts, and cardiovascular disease presentations were exclusive of patients with DM2 with maternal inheritance ( p = 0.2928, 0.1518, and 0.5237, respectively).

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