Vanzo, Rena J.
2 papers on CoChatORCID 0000-0001-7941-0106
Most cited papers
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MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways
Paciorkowski, A. R., Traylor, R. N., Rosenfeld, J. A., Hoover, J. M., Harris, C. J., Winter, S., Lacassie, Y., Bialer, M., Lamb, A. N., Schultz, R. A., et al. (2013) · neurogenetics
Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities
Cited by 109
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Disorders of creatine transport and metabolism
Longo, N., Ardon, O., Vanzo, R., Schwartz, E., & Pasquali, M. (2011) · American Journal of Medical Genetics Part C Seminars in Medical Genetics
Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism
Cited by 101
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