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Novel and recurrent mutations in the C-terminal domain of COMP cluster in two distinct regions and result in a spectrum of phenotypes within the pseudoachondroplasia - multiple epiphyseal dysplasia disease group
Kennedy, Jason; Jackson, Gail C; Barker, Faye S; Nundlall, Seema; Bella, Jordi
; et al.
Human Mutation; Hoboken Vol. 25, Iss. 6, (Jun 2005): 593-4.
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