Browsing by Author "n 2007014260"
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Homozygous mutation in MCM7 causes autosomal recessive primary microcephaly and intellectual disability
( BMJ Publishing Group , 2021 , Article)Minichromosomal maintenance (MCM) complex components 2, 4, 5 and 6 have been linked to human disease with phenotypes including microcephaly and intellectual disability. The MCM complex has DNA helicase activity and is ...
