A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis
Kisla Ekinci, Rabia Miray, Balci, Sibel, Bisgin, Atil, Altintas, Derya Ufuk, Yilmaz, MustafaLanguage:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2017.09.004
Date:
September, 2017
File:
PDF, 961 KB
english, 2017