reference/20153823

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bibliographicCitation	Stowe IB, Mercado EL, Stowe TR, Bell EL, Oses-Prieto JA, Hernández H, Burlingame AL, McCormick F. A shared molecular mechanism underlies the human rasopathies Legius syndrome and Neurofibromatosis-1. Genes Dev. 2012 Jul 01;26(13):1421–6. PMID: 22751498; PMCID: PMC3403010.
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date	2012-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A shared molecular mechanism underlies the human rasopathies Legius syndrome and Neurofibromatosis-1
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