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Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype

✍ Scribed by Brems, Hilde; Chmara, Magdalena; Sahbatou, Mourad; Denayer, Ellen; Taniguchi, Koji; Kato, Reiko; Somers, Riet; Messiaen, Ludwine; De Schepper, Sofie; Fryns, Jean-Pierre

Book ID: 109919627
Publisher: Nature Publishing Group
Year: 2007
Tongue: English
Weight: 314 KB
Volume: 39
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng2113

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