A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report

Overview of attention for article published in BMC Medical Genetics, July 2018

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Case report of TP53RK #mutation https://t.co/rJV8tu3Y9u in family with Galloway-Mowat #syndrome #raredisease https://t.co/73bwId7Sfp

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