A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report

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

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Novel WDR62 homozygous nonsense #mutation https://t.co/4hH2UZvYmS identified in patient with primary #microcephaly https://t.co/LLNdv8wL1m

A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report. https://t.co/1A9xG1UcSE https://t.co/lqVr0y41OA

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