Genotype and defects in microtubule-based motility correlate with clinical severity in KIF1A-associated neurological disorder

por Boyle, Lia, Rao, Lu, Kaur, Simranpreet, Fan, Xiao, Mebane, Caroline, Hamm, Laura, Thornton, Andrew, Ahrendsen, Jared T., Anderson, Matthew P., Christodoulou, John, Gennerich, Arne, Shen, Yufeng, Chung, Wendy K.
Publicado 2021

Availability of Services and Caregiver Burden: Supporting Individuals With Neurogenetic Conditions During the COVID-19 Pandemic

por Kowanda, Michelle, Cartner, Lindsey, Kentros, Catherine, Geltzeiler, Alexa R., Singer, Kaitlyn E., Weaver, W. Curtis, Lehman, Christopher D., Smith, Simone, Smith, Rebecca Sheedy, Walsh, Lauren Kasparson, Diehl, Katharine, Nagpal, Natalie, Brooks, Elizabeth, Mebane, Caroline M., Wilson, Ashley L., Marvin, Alison R., White, L. Casey, Law, J. Kiely, Jensen, William, Daniels, Amy M., Tjernagel, Jennifer, Snyder, LeeAnne Green, Taylor, Cora M., Chung, Wendy K.
Publicado 2021