Efthymiou, S., Salpietro, V., Bettencourt, C., & Houlden, H. (2018). Paroxysmal Movement Disorder and Epilepsy Caused by a De Novo Truncating Mutation in KAT6A. J Pediatr Genet.
Chicago ZitierstilEfthymiou, Stephanie, Vincenzo Salpietro, Conceicao Bettencourt, und Henry Houlden. "Paroxysmal Movement Disorder and Epilepsy Caused By a De Novo Truncating Mutation In KAT6A." J Pediatr Genet 2018.
MLA ZitierstilEfthymiou, Stephanie, Vincenzo Salpietro, Conceicao Bettencourt, und Henry Houlden. "Paroxysmal Movement Disorder and Epilepsy Caused By a De Novo Truncating Mutation In KAT6A." J Pediatr Genet 2018.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.