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

Bicknell, Louise S; Walker, Sarah; Klingseisen, Anna; Stiff, Tom; Leitch, Andrea; Kerzendorfer, Claudia; Martin, Carol-Anne; Yeyati, Patricia; Al Sanna, Nouriya; Bober, Michael; Johnson, Diana; Wise, Carol; Jackson, Andrew P; O'Driscoll, Mark; Jeggo, Penny

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

External DOI

https://doi.org/10.1038/ng.776

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

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

History

Publication status

Journal

ISSN

Publisher

External DOI

Issue

Volume

Page range

Department affiliated with

Notes

Full text available

Peer reviewed?

Legacy Posted Date

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