B. Chung Et Al. , "A Mutation in the Signal Sequence of LRP5 in a Family With an Osteoporosis-Pseudoglioma Syndrome (OPPG)-Like Phenotype Indicates a Novel Disease Mechanism for Trinucleotide Repeats," HUMAN MUTATION , vol.30, no.4, pp.641-648, 2009
Chung, B. Et Al. 2009. A Mutation in the Signal Sequence of LRP5 in a Family With an Osteoporosis-Pseudoglioma Syndrome (OPPG)-Like Phenotype Indicates a Novel Disease Mechanism for Trinucleotide Repeats. HUMAN MUTATION , vol.30, no.4 , 641-648.
Chung, B., Kayserili, H., Ai, M., Freudenberg, J., Uezmcue, A., Uyguner, O., ... Bartels, C. F.(2009). A Mutation in the Signal Sequence of LRP5 in a Family With an Osteoporosis-Pseudoglioma Syndrome (OPPG)-Like Phenotype Indicates a Novel Disease Mechanism for Trinucleotide Repeats. HUMAN MUTATION , vol.30, no.4, 641-648.
Chung, Boi-Dinh Et Al. "A Mutation in the Signal Sequence of LRP5 in a Family With an Osteoporosis-Pseudoglioma Syndrome (OPPG)-Like Phenotype Indicates a Novel Disease Mechanism for Trinucleotide Repeats," HUMAN MUTATION , vol.30, no.4, 641-648, 2009
Chung, Boi-Dinh Et Al. "A Mutation in the Signal Sequence of LRP5 in a Family With an Osteoporosis-Pseudoglioma Syndrome (OPPG)-Like Phenotype Indicates a Novel Disease Mechanism for Trinucleotide Repeats." HUMAN MUTATION , vol.30, no.4, pp.641-648, 2009
Chung, B. Et Al. (2009) . "A Mutation in the Signal Sequence of LRP5 in a Family With an Osteoporosis-Pseudoglioma Syndrome (OPPG)-Like Phenotype Indicates a Novel Disease Mechanism for Trinucleotide Repeats." HUMAN MUTATION , vol.30, no.4, pp.641-648.
@article{article, author={Boi-Dinh Chung Et Al. }, title={A Mutation in the Signal Sequence of LRP5 in a Family With an Osteoporosis-Pseudoglioma Syndrome (OPPG)-Like Phenotype Indicates a Novel Disease Mechanism for Trinucleotide Repeats}, journal={HUMAN MUTATION}, year=2009, pages={641-648} }