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A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy https://t.co/O5LFUJYTws https://t.co/aiVD25MVvI
A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy https://t.co/O5LFUJYTws https://t.co/aiVD25MVvI
New Research: A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy: Objective Global developmental delay has markedly high phenotypic and genetic heterogeneity, and is a great… https://t.co/H