Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy von Koko, Mahmoud, Elseed, Maha A., Mohammed, Inaam N., Hamed, Ahlam A., Abd Allah, Amal S. I., Yahia, Ashraf, Siddig, Rayan A., Altmüller, Janine, Toliat, Mohammad Reza, Elmahdi, Esra O., Amin, Mutaz, Ahmed, Elhami A., Eltazi, Isra Z. M., Elmugadam, Fatima A., Abdelgadir, Wasma A., Eltaraifee, Esraa, Ibrahim, Mohamed O. M., Ali, Nabila M. H., Malik, Hiba M., Babai, Arwa M., Bakhit, Yousuf H., Nürnberg, Peter, Ibrahim, Muntaser E., Salih, Mustafa A., Schubert, Julian, Elsayed, Liena E. O., Lerche, Holger

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Comparison of autism domains across thirty rare variant genotypes von Ali, Nabila M.H., Chawner, Samuel J.R.A., Kushan-Wells, Leila, Bearden, Carrie E., Mulle, Jennifer Gladys, Pollak, Rebecca M., Gur, Raquel E., Chung, Wendy K., Housby, Harriet, Lee, Irene, Skuse, David, Wolstencroft, Jeanne, Mandy, William, Denaxas, Spiros, Baker, Kate, Raymond, Lucy, van den Bree, Marianne, Chawner, Samuel, Hall, Jeremy, Holmans, Peter, Hope-Bell, Josh, Le Roux, Danielle, Morrin, Sally, Owen, Michael, Sivakumar, Shreeya, Owen, Michael J., van den Bree, Marianne B.M.

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Comparison of autism domains across thirty rare variant genotypesResearch in context von Nabila M.H. Ali, Samuel J.R.A. Chawner, Leila Kushan-Wells, Carrie E. Bearden, Jennifer Gladys Mulle, Rebecca M. Pollak, Raquel E. Gur, Wendy K. Chung, Michael J. Owen, Marianne B.M. van den Bree, Harriet Housby, Irene Lee, David Skuse, Jeanne Wolstencroft, William Mandy, Spiros Denaxas, Kate Baker, Lucy Raymond, Marianne van den Bree, Samuel Chawner, Jeremy Hall, Peter Holmans, Josh Hope-Bell, Danielle Le Roux, Sally Morrin, Michael Owen, Shreeya Sivakumar

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