Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study.

Autor: Małachowska, Beata1 (AUTHOR), Janikiewicz, Justyna2 (AUTHOR), Pietrowska, Karolina3 (AUTHOR), Wyka, Krystyna4 (AUTHOR), Madzio, Joanna4 (AUTHOR), Wypyszczak, Kamila4 (AUTHOR), Tkaczyk, Marcin5,6 (AUTHOR), Chrul, Sławomir5 (AUTHOR), Zwiech, Rafał7 (AUTHOR), Hogendorf, Anna8 (AUTHOR), Małecki, Maciej T.9 (AUTHOR), Borowiec, Maciej10 (AUTHOR), Krętowski, Adam3,11 (AUTHOR), Młynarski, Wojciech4 (AUTHOR), Dobrzyń, Agnieszka2 (AUTHOR), Ciborowski, Michał3 (AUTHOR), Fendler, Wojciech1,12 (AUTHOR) wojciech.fendler@umed.lodz.pl
Zdroj: Metabolomics. Mar2022, Vol. 18 Issue 3, p1-12. 12p.
Databáze: Academic Search Ultimate
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