A Clinical Case of Patient Carrying Rare Pathological PSEN1 Gene Mutation (L424V) Demonstrates the Phenotypic Heterogenity of Early Onset Familial AD

por Stoychev, Kaloyan R., Stoimenova-Popova, Maya, Chumpalova, Petranka, Ilieva, Lilia, Swamad, Mohamed, Kamburova-Martinova, Zornitsa
Publicado 2019