Bicknell LS

ORCID: 0000-0001-6899-9322 · 1 paper in corpus

2021

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

European journal of human genetics : EJHG ·doi:10.1038/s41431-021-00839-4

The MCM2-7 helicase is a heterohexameric complex with essential roles as part of both the pre-replication and pre-initiation complexes in the early stages of DNA replication. Meier-Gorlin syndrome, a rare primordial dwarfism, is strongly as…