Case report: A de novo RASopathy-causing SHOC2 variant in a Chinese girl with noonan syndrome-like with loose anagen hair

Overview of attention for article published in Frontiers in Genetics, December 2022

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New Research: Case report: A de novo RASopathy-causing SHOC2 variant in a Chinese girl with noonan syndrome-like with loose anagen hair: Pathogenic variants in the RASopathy-causing SHOC2 gene have been suggested to cause Noonan syndrome-like… https://t.co

09 Dec 2022

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