7CB69A75-A37A-45E9-BA88-4EBF757E4A6AUse of patient mis sense mutations in SCN9A to increase our understanding of the structure and function of sodium channelsStudentship18014062512EF1C-401B-4222-9869-A770D4C5FAC7BBSRCINCOME_ACTUAL06FB44182-70BD-4A87-974D-C5036276095CExtending the phenotype of midface toddler excoriation syndrome (MiTES): Five new cases in three families with PR domain containing protein 12 (PRDM12) mutations.Journal of the American Academy of Dermatology0131b742ecd303b20915e7b6dfcf105fInamadar AC2019-01-01http://dx.doi.org/10.1016/j.jaad.2019.05.03631128170http://ukpmc.ac.uk/abstract/MED/311281700190-9622http://europepmc.org/abstract/MED/31128170816Journal Article/Review5e6a5ae3845321.42586928