A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis
| Autor: | Kisla Ekinci, Rabia Miray, Balci, Sibel, Bisgin, Atil, Altintas, Derya Ufuk, Yilmaz, Mustafa |
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| Zdroj: | In European Journal of Medical Genetics December 2017 60(12):690-694 |
| Databáze: | ScienceDirect |
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