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The phenotype of compound heterozygous BSEP deficiency pati..:
Felzen, Antonia
;
van Wessel, Daan
;
Thompson, Richard
...
Journal of Hepatology. 73 (2020) - p. S536-S537 , 2020
Link:
https://doi.org/10.1016/s0168-8278(20)31546-4
RT Journal T1
The phenotype of compound heterozygous BSEP deficiency patients is determined by the combined residual function of the two ABCB11 mutations: results from the NAPPED consortium
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_s0168-8278(20)31546-4&Exemplar=1&LAN=DE A1 Felzen, Antonia A1 van Wessel, Daan A1 Thompson, Richard A1 Gonzales, Emmanuel A1 Jankowska, Irena A1 Sokal, Etienne A1 Grammatikopoulos, Tassos A1 Kadaristiana, Agustina A1 Jacquemin, Emmanuel A1 Spraul, Anne A1 Lipiński, Patryk A1 Czubkowski, Piotr A1 Rock, Nathalie A1 Shagrani, Mohammad Ali A1 Broering, Dieter Clemens A1 Algoufi, Talal A1 Mazhar, Nejat A1 Nicastro, Emanuele A1 Kelly, Deirdre A1 Nebbia, Gabriella A1 Arnell, Henrik A1 Fischler, Björn A1 Hulscher, JBF A1 Serranti, Daniele A1 Arıkan, Cigdem A1 Polat, Esra A1 Debray, Dominique A1 Lacaille, Florence A1 Gonçalves, Cristina A1 Hierro, Loreto PB Elsevier BV YR 2020 SN 0168-8278 JF Journal of Hepatology VO 73 SP S536 OP S537 LK http://dx.doi.org/https://doi.org/10.1016/s0168-8278(20)31546-4 DO https://doi.org/10.1016/s0168-8278(20)31546-4 SF ELIB - SuUB Bremen
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