The first Turkish family with the diagnosis of retinal vasculopathy with cerebral leukodystrophy (RVCL) where a new mutation was found
Autor: | Bademkiran, F., Nalcaci, S., Eraslan, C., Durmaz, A. |
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Zdroj: | In Journal of the Neurological Sciences 15 October 2017 381 Supplement:378-379 |
Databáze: | ScienceDirect |
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