Kurolap, A. Et Al. 2022. Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity. AMERICAN JOURNAL OF HUMAN GENETICS , vol.109, no.3 , 518-532.

Kurolap, A., Kreuder, F., Gonzaga-Jauregui, C., Duvdevani, M. P., Harel, T., Tammer, L., ... Xin, B.(2022). Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity. AMERICAN JOURNAL OF HUMAN GENETICS , vol.109, no.3, 518-532.

Kurolap, Alina Et Al. "Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity," AMERICAN JOURNAL OF HUMAN GENETICS , vol.109, no.3, 518-532, 2022

Kurolap, Alina Et Al. "Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity." AMERICAN JOURNAL OF HUMAN GENETICS , vol.109, no.3, pp.518-532, 2022

Kurolap, A. Et Al. (2022) . "Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity." AMERICAN JOURNAL OF HUMAN GENETICS , vol.109, no.3, pp.518-532.

@article{article, author={Alina Kurolap Et Al. }, title={Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2022, pages={518-532} }