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Autor:
Danique van Vliet, Willem G. van Ginkel, Els van der Goot, Eddy A. van der Zee, Francjan J. van Spronsen, Martijn H. J. R. Faassen, Arndt Vogel, M. Rebecca Heiner-Fokkema
Publikováno v:
Nutrients
Nutrients, Vol 11, Iss 10, p 2486 (2019)
Volume 11
Issue 10
Nutrients, 11(10):2486. MDPI AG
Nutrients, Vol 11, Iss 10, p 2486 (2019)
Volume 11
Issue 10
Nutrients, 11(10):2486. MDPI AG
Tyrosinemia type 1 (TT1) is a rare metabolic disease caused by a defect in the tyrosine degradation pathway. Neurocognitive deficiencies have been described in TT1 patients, that have, among others, been related to changes in plasma large neutral ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc79a9f87854adddd5c6242e8d4653cb
https://doi.org/10.3390/nu11102486
https://doi.org/10.3390/nu11102486
