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

✍ Scribed by Bicknell, Louise S; Walker, Sarah; Klingseisen, Anna; Stiff, Tom; Leitch, Andrea; Kerzendorfer, Claudia; Martin, Carol-Anne; Yeyati, Patricia; Al Sanna, Nouriya; Bober, Michael


Book ID
109914721
Publisher
Nature Publishing Group
Year
2011
Tongue
English
Weight
905 KB
Volume
43
Category
Article
ISSN
1061-4036

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