Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype
Nature Genetics2007Vol. 39(9), pp. 1120–1126
Citations Over TimeTop 1% of 2007 papers
Hilde Brems, Magdalena Chmara, Mourad Sahbatou, Ellen Denayer, Koji Taniguchi, Reiko Kato, Riet Somers, Ludwine Messiaen, Sofie De Schepper, Jean‐Pierre Fryns, Jan Cools, Peter Marynen, Gilles Thomas, Akihiko Yoshimura, Eric Legius
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