Identification of a human-specific epitope in a conserved region of the La/SS-B autoantigen.

par Weng, Y M, McNeilage, J, Topfer, F, McCluskey, J, Gordon, T
Publié 1993

A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia.

par Chan, D, Weng, Y M, Graham, H K, Sillence, D O, Bateman, J F
Publié 1998