Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder

Overview of attention for article published in Frontiers in endocrinology, September 2019

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New Research: Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder: Context: MIRAGE (Myelodysplasia, Infection, Restriction of growth, Adrenal hypoplasia,… https://t.co/hwSpCJez

11 Sep 2019

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