Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1
Dominic Lenz(Heidelberg University), Christian Staufner(Heidelberg University), Jennifer E. Posey(MACOM (United States)), Desirée E.C. Smith(Amsterdam Neuroscience), Claire Reynolds(Children's Health Ireland at Crumlin), Julian Schröter(Heidelberg University), Tobias B. Haack(Technical University of Munich), Saskia B. Wortmann(Paracelsus Medical University), D. Caldari(Centre Hospitalier Universitaire de Nantes), Ellen Crushell(Temple Street Children's University Hospital), Nicola Dikow(Heidelberg University), Sébastien Küry(Génétique Médicale & Génomique Fonctionelle), Gajja S. Salomons(University Medical Center), Bader Alhaddad(Helmholtz Zentrum München), Denise Horn(Charité - Universitätsmedizin Berlin), Jill A. Rosenfeld(Baylor College of Medicine), Urania Kotzaeridou(Heidelberg University), Lucia Laugwitz(University Children's Hospital Tübingen), Saskia Biskup(Praxis für Humangenetik Tübingen), Inga Harting(Heidelberg University), Holger Prokisch(Helmholtz Zentrum München), Matias Wagner(Helmholtz Zentrum München), Bruce H. R. Wolffenbuttel(University Medical Center Groningen), Bertrand Isidor(Centre National de la Recherche Scientifique), Alyssa Bianzano(Heidelberg University), Elke Lainka(University of Duisburg-Essen), Simone Kathemann(ThyssenKrupp (Germany)), Heiko Brennenstuhl(Heidelberg University), Fleur Vansenne(University Medical Center Groningen), Robert Kopajtich(Helmholtz Zentrum München), Claudia Weiß(RWTH Aachen University), Georg F. Hoffmann(Laboratoire des Sciences du Climat et de l'Environnement), Joanne Hughes(Children's Health Ireland at Crumlin), Andrea Hanson‐Kahn(Stanford Medicine), Marisa I. Mendes(Amsterdam Neuroscience), Jonathan A. Bernstein(Lucile Packard Children's Hospital), Stefan Kölker(Heidelberg University), James R. Lupski(Baylor College of Medicine), M. Huijberts(University Medical Center Groningen), Ralf A. Husain
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