Export 1 results:
Author Title Type [ Year
] Filters: Keyword is Carrier Proteins and Author is Vidal, Enrique [Clear All Filters]
Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype. Hum Genet. 2016;135(12):1343-1354. doi:10.1007/s00439-016-1721-3.