Schlieben, L. D. Et Al. 2023. The PALFES study: exome sequencing identified the genetic cause in 40% of 256 pediatric acute liver failure cases without aetiology. EUROPEAN JOURNAL OF HUMAN GENETICS , 32-33.

Schlieben, L. D., Lenz, D., Shimura, M., Bianzano, A., Smirnov, D., Kopajtich, R., ... Adam, R.(2023). The PALFES study: exome sequencing identified the genetic cause in 40% of 256 pediatric acute liver failure cases without aetiology. EUROPEAN JOURNAL OF HUMAN GENETICS , 32-33.

Schlieben, Lea Et Al. "The PALFES study: exome sequencing identified the genetic cause in 40% of 256 pediatric acute liver failure cases without aetiology," EUROPEAN JOURNAL OF HUMAN GENETICS , 32-33, 2023

Schlieben, Lea D. Et Al. "The PALFES study: exome sequencing identified the genetic cause in 40% of 256 pediatric acute liver failure cases without aetiology." EUROPEAN JOURNAL OF HUMAN GENETICS , pp.32-33, 2023

Schlieben, L. D. Et Al. (2023) . "The PALFES study: exome sequencing identified the genetic cause in 40% of 256 pediatric acute liver failure cases without aetiology." EUROPEAN JOURNAL OF HUMAN GENETICS , pp.32-33.

@article{article, author={Lea Dewi Schlieben Et Al. }, title={The PALFES study: exome sequencing identified the genetic cause in 40% of 256 pediatric acute liver failure cases without aetiology}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2023, pages={32-33} }