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Autor:
Margret Heddrich-Ellerbrok, Vanessa Korpel, Carmen Rohde, Anibh M. Das, Katharina Dokoupil, Dinah Lier, Dorothea Möslinger, Stephan vom Dahl, Aleksandra Fischer, U. Meyer, Friederike Bärhold, Skadi Beblo, Eva Thimm, Sebene Mayorandan, Stefanie Rosenbaum-Fabian, Agnes van Teeffelen-Heithoff, Janina Lahl, Anne-Kathrin Neugebauer, Anna Fekete, Nina Bogovic, Monika Jörg-Streller, Michel Hochuli, Peter Freisinger, Ulrike Och
Publikováno v:
Nutrients
Nutrients, Vol 13, Iss 134, p 134 (2021)
Volume 13
Issue 1
Nutrients, Vol 13, Iss 134, p 134 (2021)
Volume 13
Issue 1
Background: Tyrosinaemia type 1 is a rare inherited metabolic disease caused by an enzyme defect in the tyrosine degradation pathway. It is treated using nitisinone and a low-protein diet. In a workshop in 2013, a group of nutritional specialists fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::668eb34e15bb299b6fa18cc6ad57511d
https://doi.org/10.3390/nu13010134
https://doi.org/10.3390/nu13010134
