Stotz, Stephanie C.

CACNA1H mutations in autism spectrum disorders

Splawski, I., Yoo, D. S., Stotz, S. C., Cherry, A., Clapham, D. E., & Keating, M. T. (2006) · Journal of Biological Chemistry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

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A common haplotype containing functional CACNA1H variants is frequently coinherited with increased TPSAB1 copy number

Lyons, J. J., Stotz, S. C., Chovanec, J., Liu, Y., Lewis, K. L., Nelson, C., DiMaggio, T., Jones, N., Stone, K. D., Sung, H., et al. (2018) · Genetics in Medicine

Ion channel regulation and functionGenetic Associations and Epidemiology

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