J. Ravell Et Al. , "Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease," JOURNAL OF CLINICAL INVESTIGATION , vol.130, no.1, pp.507-522, 2020
Ravell, J. Et Al. 2020. Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease. JOURNAL OF CLINICAL INVESTIGATION , vol.130, no.1 , 507-522.
Ravell, J., Matsuda-Lennikov, M., Chauvin, S., Zou, J., Biancalana, M., Deeb, S., ... Price, S.(2020). Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease. JOURNAL OF CLINICAL INVESTIGATION , vol.130, no.1, 507-522.
Ravell, JC Et Al. "Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease," JOURNAL OF CLINICAL INVESTIGATION , vol.130, no.1, 507-522, 2020
Ravell, JC Et Al. "Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease." JOURNAL OF CLINICAL INVESTIGATION , vol.130, no.1, pp.507-522, 2020
Ravell, J. Et Al. (2020) . "Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease." JOURNAL OF CLINICAL INVESTIGATION , vol.130, no.1, pp.507-522.
@article{article, author={JC Ravell Et Al. }, title={Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease}, journal={JOURNAL OF CLINICAL INVESTIGATION}, year=2020, pages={507-522} }