Nutritional, muscular and metabolic characteristics in patients with neurofibromatosis type 1
Author:
Affiliation:
1. Department of Dermatology; Faculty of Medicine; Fukuoka University; Fukuoka Japan
2. Department of Medicine of Sensory and Motor Organs; Division of Dermatology; Faculty of Medicine; Tottori University; Tottori Japan
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.13218/fullpdf
Reference18 articles.
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2. The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation;Tidyman;Curr Opin Genet Dev,2009
3. Germline loss-of-function mutation in SPRED1 cause a neurofibromatosis 1-like phenotype;Brems;Nat Genet,2007
4. Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome;Messiaen;JAMA,2009
5. Clinical features and pathobiology of neurofibromatosis 1;Korf;J Child Neurol,2002
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