Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function
Cortés, Claudio R., McInerney-Leo, Aideen M., Vogel, Ida, Rondón Galeano, Maria C., Leo, Paul J., Harris, Jessica E., Anderson, Lisa K., Keith, Patricia A., Brown, Matthew A., Ramsing, Mette, Duncan,Volume:
6
Langue:
english
Journal:
Scientific Reports
DOI:
10.1038/srep24083
Date:
April, 2016
Fichier:
PDF, 1.35 MB
english, 2016