Cousin, Margot A.
Mayo Clinic
2 papers on CoChatORCID 0000-0002-6119-9346
Most cited papers
- Verified
Bi-allelic alterations in AEBP1 lead to defective collagen assembly and connective tissue structure resulting in a variant of Ehlers-Danlos syndrome
Blackburn, P. R., Xu, Z., Tumelty, K. E., Zhao, R. W., Monis, W. J., Harris, K. G., Gass, J. M., Cousin, M. A., Boczek, N. J., Mitkov, M. V., et al. (2018) · The American Journal of Human Genetics
Connective tissue disorders researchDermatological and Skeletal Disorders
Cited by 176
- Verified
Variants in DOCK3 cause developmental delay and hypotonia
Wiltrout, K., Ferrer, A., van de Laar, I., Namekata, K., Harada, T., Klee, E. W., Zimmerman, M. T., Cousin, M. A., Kempainen, J. L., Babovic-Vuksanovic, D., et al. (2019) · European Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 17
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