Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome

Overview of attention for article published in Clinical Epigenetics, May 2020

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RT @angfaber: Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome. https://t.co/q…

Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome. https://t.co/quFCD7hrxW #longqt #cardiotwitter #epeeps

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