The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post‐mortem.

Autor: Forsyth, RaeLynn, Peretz, Ryan H., Dempsey, Angela, Britton, Jacquelyn, Kratz, Lisa, Hamosh, Ada, Vernon, Hilary, Batshaw, Mark L., Valle, David
Zdroj: Journal of Inherited Metabolic Disease Reports; May2023, Vol. 64 Issue 3, p233-237, 5p
Databáze: Complementary Index
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