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Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.

journal contribution
posted on 2023-06-07, 23:37 authored by Louise S Bicknell, Sarah Walker, Anna Klingseisen, Tom Stiff, Andrea Leitch, Claudia Kerzendorfer, Carol-Anne Martin, Patricia Yeyati, Nouriya Al Sanna, Michael Bober, Diana Johnson, Carol Wise, Andrew P Jackson, Mark O'DriscollMark O'Driscoll, Penny Jeggo
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History

Publication status

  • Published

Journal

Nature Genetics

ISSN

1061-4036

Publisher

Nature Publishing Group

Issue

4

Volume

43

Page range

350-355

Department affiliated with

  • Sussex Centre for Genome Damage Stability Publications

Notes

This article was featured on the journal cover.

Full text available

  • No

Peer reviewed?

  • Yes

Legacy Posted Date

2012-02-06

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