Cockayne syndrome caused by paternally inherited 5 Mb deletion of 10q11.2 and a frameshift mutation of ERCC6
Shailly Jain Ghai, Mary Shago, Manohar Shroff, Grace YoonVolume:
54
Year:
2011
Language:
english
Pages:
277
DOI:
10.1016/j.ejmg.2011.02.008
File:
PDF, 424 KB
english, 2011