Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome
2011; Nature Portfolio; Volume: 43; Issue: 4 Linguagem: Inglês
10.1038/ng.776
ISSN1546-1718
AutoresLouise S. Bicknell, Sarah Walker, Anna Klingseisen, Tom Stiff, Andrea Leitch, Claudia Kerzendorfer, Carol-Anne Martin, Patricia L. Yeyati, Nouriya Al Sanna, Michael B. Bober, Diana Johnson, Carol A. Wise, Andrew P. Jackson, Mark O’Driscoll, Penny A. Jeggo,
Tópico(s)Genetic and Kidney Cyst Diseases
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