The PALFES study: exome sequencing identified the genetic cause in 40% of 256 pediatric acute liver failure cases without aetiology

Schlieben, Lea Dewi and Lenz, Dominic and Shimura, Masaru and Bianzano, Alyssa and Smirnov, Dmitrii and Kopajtich, Robert and Adam, Rudiger and Vogel, Georg-Friedrich and Baric, Ivo and Bufler, Philip and Burnyte, Birute and Calvo, Pier Luigi and Crushell, Ellen and Das, Anibh M. and Distelmaier, Felix and Freisinger, Peter and Hadzic, Nedim and Hartleif, Steffen and Hempel, Maja and Kansu, Aydan and Kaspar, Sonja and Kelly, Deidre and Knoppke, Birgit and Konstantopoulou, Vassiliki and Krylova, Tatiana and Alice, Kuster and Lainka, Elke and Lurz, Eberhard and Mandel, Hanna and McKiernan, Patrick and Piekutowska-Abramczuk, Dorota and Rotig, Agnes and Santer, Rene and Taylor, Robert and Wortmann, Saskia and Vockley, Jerry and Koelker, Stefan and Hoffmann, Georg Friedrich and Meitinger, Thomas and Murayama, Kei and Staufner, Christian and Prokisch, Holger (2023) The PALFES study: exome sequencing identified the genetic cause in 40% of 256 pediatric acute liver failure cases without aetiology. In: 55th European-Society of Human Genetics (ESHG) Conference, June 11-14, 2022, Vienna, Austria.

Full text not available from this repository.

Item Type:	Conference or Workshop Item (Speech)
Subjects:	600 Technology > 610 Medical sciences Medicine
Divisions:	Medicine > Lehrstuhl für Kinder- und Jugendmedizin
Depositing User:	Dr. Gernot Deinzer
Date Deposited:	05 Mar 2024 07:38
Last Modified:	05 Mar 2024 07:38
URI:	https://pred.uni-regensburg.de/id/eprint/60923

Actions (login required)

View Item