Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
Immacolata Andolfo(Ceinge Biotecnologie Avanzate (Italy)), Achille Iolascon(Ceinge Biotecnologie Avanzate (Italy)), Gordon W. Stewart(University College London), Carlo Brugnara(Boston Children's Hospital), Lucia De Franceschi(University of Verona), J. Delaunay(Université Paris-Sud), Rupa Narayan(Stanford University), Fara Vallefuoco(University of Naples Federico II), Orsetta Zuffardi(University of Pavia), Carla Auriemma(University of Naples Federico II), Annalisa Vetro(University of Pavia), Maria Rosaria Esposito(University of Naples Federico II), Luigia De Falco(University of Naples Federico II), Ivan Limongelli(University of Pavia), Boris E. Shmukler(Beth Israel Deaconess Medical Center), Roberta Russo(Ceinge Biotecnologie Avanzate (Italy)), Donatella Montanaro(University of Naples Federico II), Maria DʼArmiento(University of Naples Federico II), David H. Vandorpe(Beth Israel Deaconess Medical Center), Seth L. Alper(Beth Israel Deaconess Medical Center), Stanley L. Schrier(Stanford University), Bertil Glader(Stanford University)
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