Referee report. For: Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive [version 1; referees: 2 approved]

Sulman Basit
Text published 2018 via F1000 Research Limited
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https://doi.org/10.5256/f1000research.13096.r29314 Cite
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