Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings
Caylor, R. C., Grote, L., Thiffault, I., Farrow, E. G., Willig, L., Soden, S., Amudhavalli, S. M., Nopper, A. J., Horii, K. A., Fleming, E., Jenkins, J., Welsh, H., Ilyas, M., Engleman, K., Abdelmoity, A., Saunders, C. J.
Published in Neurogenetics (01.08.2018)
Published in Neurogenetics (01.08.2018)
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