Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9
Noah C. Helderman(Leiden University Medical Center), Maartje Nielsen(University Medical Center Groningen), Claire Palles(University of Oxford), Leendert H. J. Looijenga(University Medical Center Utrecht), Inge M. M. Lakeman(Leiden University Medical Center), Frederik J. Hes(Leiden University Medical Center), Marjolijn C.J. Jongmans(Utrecht University), Frank Tüttelmann(Institute of Human Genetics), Johanna Steingröver(University Hospital Münster), Richarda M. de Voer(Radboud University Nijmegen), Sergi Castellvı́-Bel(Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas), Tom van Wezel(Leiden University Medical Center), Davy Cats(Leiden University Medical Center), Annelore Van Der Kelen(Universitair Ziekenhuis Brussel), Marry M. van den Heuvel‐Eibrink(Princess Máxima Center), Yael Goldberg(Rabin Medical Center), Ting Yang(Nantong University), Laia Bonjoch(Institut d'Investigacions Biomèdiques de Barcelona), Irma van de Beek(Amsterdam University Medical Centers), Sabine Kliesch(University Hospital Münster), Margot J. Wyrwoll(MRC Centre for Regenerative Medicine), Hailiang Mei, Roland P. Kuiper(Princess Máxima Center), Diantha Terlouw(Leiden University Medical Center), Marina Gay(Institute for Research in Biomedicine), Laura Valle(Institut d'Investigació Biomédica de Bellvitge), Ruben H.P. Vorderman(Leiden University Medical Center), Mariano Golubicki, Dineke Westra(Radboud University Nijmegen), Manon S. Oud(Radboud University Nijmegen), Ludmil B. Alexandrov(UC San Diego Health System), Hans Morreau(Leiden University Medical Center), Thomas F. Eleveld(Princess Máxima Center), Andrew Green(Newcastle University), Marina Antelo, Lisa E.E.L.O. Lashley(Leiden University Medical Center), Ashwin Ramdien(Leiden University Medical Center), Yardena Tenenbaum‐Rakover(Rappaport Family Institute for Research in the Medical Sciences), Carli M.J. Tops(State University of New York), Mariona Terradas(Universitat Autònoma de Barcelona)
Cited by 1
Related Papers
Signatures of mutational processes in human cancer
|Nature|2013|10.1k
The repertoire of mutational signatures in human cancer
|Nature|2020|3.8k
Pan-cancer analysis of whole genomes
|Nature|2020|3.3k
Patterns of somatic mutation in human cancer genomes
|Nature|2007|3.1k