Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report

Overview of attention for article published in BMC Neurology, February 2020

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Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report. https://t.co/BUhgHYf03b

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