Disruption of KCNQ1 prevents methylation of the ICR2 and supports the hypothesis that its transcription is necessary for imprint establishment

Overview of attention for article published in European Journal of Human Genetics, February 2019

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RT @ejhg_journal: #BeckwithWiedemannsyndrome is associated with hypomethylation at ICR2, which is within KCNQ1 gene. This paper suggests t…

RT @ejhg_journal: #BeckwithWiedemannsyndrome is associated with hypomethylation at ICR2, which is within KCNQ1 gene. This paper suggests t…

RT @ejhg_journal: #BeckwithWiedemannsyndrome is associated with hypomethylation at ICR2, which is within KCNQ1 gene. This paper suggests t…

RT @ejhg_journal: #BeckwithWiedemannsyndrome is associated with hypomethylation at ICR2, which is within KCNQ1 gene. This paper suggests t…

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