MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency

Overview of attention for article published in European Journal of Human Genetics, March 2021

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In the top 25% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (84th percentile)
High Attention Score compared to outputs of the same age and source (82nd percentile)

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twitter: 13 X users

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Defects in DNA replication cause small brain size and short stature in people with Meier-Gorlin syndrome #RareDiseaseDay2022 https://t.co/9gREthDGsz

RT @ejhg_journal: Clinical phenotypes associated with bi-allelic variants in members of the MCM2-7 helicase complex. @bicknell_l https://…

Clinical phenotypes associated with bi-allelic variants in members of the MCM2-7 helicase complex. @bicknell_l https://t.co/XN3vF5NNmB

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