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Targeted/exome sequencing identified mutations in ten Chinese patients diagnosed with Noonan syndrome and related disorders

Abstract Background Noonan syndrome (NS) and Noonan syndrome with multiple lentigines (NSML) are autosomal dominant developmental disorders. NS and NSML are caused by abnormalities in genes that encode proteins related to the RAS-MAPK pathway, including PTPN11, RAF1, BRAF, and MAP2K. In this study,...

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Main Authors:	Shanshan Xu (Author), Yanjie Fan (Author), Yu Sun (Author), Lili Wang (Author), Xuefan Gu (Author), Yongguo Yu (Author)
Format:	Book
Published:	BMC, 2017-10-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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