Viskochil, David

The neurofibromatosis type 1 gene encodes a protein related to GAP

Xu, G., O'Connell, P., Viskochil, D., Cawthon, R., Robertson, M., Culver, M., Dunn, D., Stevens, J., Gesteland, R., White, R., et al. (1990) · Cell

Neurofibromatosis and Schwannoma CasesProtein Tyrosine Phosphatases

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Diazoxide choline extended-release tablet in people with Prader-Willi syndrome: a double-blind, placebo-controlled trial

Miller, J. L., Gevers, E., Bridges, N., Yanovski, J. A., Salehi, P., Obrynba, K. S., Felner, E. I., Bird, L. M., Shoemaker, A. H., Angulo, M., et al. (2023) · The Journal of Clinical Endocrinology & Metabolism

Genetic Syndromes and ImprintingRegulation of Appetite and Obesity

Cited by 55

Deep phenotyping of patients with Tuberous Sclerosis Complex and no mutation identified in TSC1 and TSC2

Peron, A., Vignoli, A., Briola, F. L., Morenghi, E., Tansini, L., Alfano, R. M., Bulfamante, G., Terraneo, S., Ghelma, F., Banderali, G., et al. (2018) · European Journal of Medical Genetics

Tuberous Sclerosis Complex ResearchGenetic and rare skin diseases.

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