Michels, S. Et Al. 2017. Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.173, no.12 , 3127-3131.

Michels, S., Foss, K., Park, K., Golden-Grant, K., Saneto, R., Lopez, J., ... Mirzaa, G. M.(2017). Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.173, no.12, 3127-3131.

Michels, Savannah Et Al. "Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.173, no.12, 3127-3131, 2017

Michels, Savannah Et Al. "Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.173, no.12, pp.3127-3131, 2017

Michels, S. Et Al. (2017) . "Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.173, no.12, pp.3127-3131.

@article{article, author={Savannah Michels Et Al. }, title={Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2017, pages={3127-3131} }