DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Brems H, Chmara M, Sahbatou M. , et al.
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.
Nat Genet 2007;
39 (09) 1120-1126
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