Αρχειοθήκη ιστολογίου

Παρασκευή 15 Σεπτεμβρίου 2017

A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review

Progranulin gene (GRN) mutations are major causes of frontotemporal lobar degeneration. To date, 68 pathogenic GRN mutations have been identified. However, very few of these mutations have been reported in Asians...

from #ORL-AlexandrosSfakianakis via ola Kala on Inoreader http://ift.tt/2x3vI82

Δεν υπάρχουν σχόλια:

Δημοσίευση σχολίου