Kim, A. H. Et Al. 2024. CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. LIFE SCIENCE ALLIANCE , vol.7, no.10 , 1-10.

Kim, A. H., Sakin, I., Vivano, S., Tuncel, G., Aguilera, S. M., Goles, G., ... Jeffries, L.(2024). CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. LIFE SCIENCE ALLIANCE , vol.7, no.10, 1-10.

Kim, Angelina Et Al. "CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow," LIFE SCIENCE ALLIANCE , vol.7, no.10, 1-10, 2024

Kim, Angelina H. Et Al. "CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow." LIFE SCIENCE ALLIANCE , vol.7, no.10, pp.1-10, 2024

Kim, A. H. Et Al. (2024) . "CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow." LIFE SCIENCE ALLIANCE , vol.7, no.10, pp.1-10.

@article{article, author={Angelina Haesoo Kim Et Al. }, title={CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow}, journal={LIFE SCIENCE ALLIANCE}, year=2024, pages={1-10} }