Review and update ofSPRED1mutations causing legius syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22152/fullpdf
Reference48 articles.
1. Does SPRED1 contribute to leukemogenesis in juvenile myelomonocytic leukemia (JMML)?;Batz;Blood,2010
2. Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1;Brems;Lancet Oncol,2009
3. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype;Brems;Nat Genet,2007
4. Getting a first clue about SPRED functions;Bundschu;Bioessays,2007
5. A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay;Chen;Eur J Med Genet,2008
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