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Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype
2007
471 citations
Journal Article
Field-Weighted Citation Impact:
11.11
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype | Researchclopedia
Ludwine Messiaen
·
University of Alabama at Birmingham
Sofie De Schepper
·
Ghent University Hospital
Jean‐Pierre Fryns
·
KU Leuven
Jan Cools
·
KU Leuven
Peter Marynen
·
Vlaams Instituut voor Biotechnologie
Gilles Thomas
·
Fondation Jean Dausset-CEPH
Akihiko Yoshimura
·
Kyushu University
Eric Legius
·
KU Leuven