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RT @FrontGenetics: New Research: A De Novo Mutation in DYRK1A Causes Syndromic Intellectual Disability: A Chinese Case Report: Autosomal do…
RT @FrontGenetics: New Research: A De Novo Mutation in DYRK1A Causes Syndromic Intellectual Disability: A Chinese Case Report: Autosomal do…
RT @FrontGenetics: New Research: A De Novo Mutation in DYRK1A Causes Syndromic Intellectual Disability: A Chinese Case Report: Autosomal do…
New Research: A De Novo Mutation in DYRK1A Causes Syndromic Intellectual Disability: A Chinese Case Report: Autosomal dominant mental retardation-7 (MRD7) is a rare anomaly, characterized by severe intellectual disability, feeding difficulties,… https://t.