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Whole-exome Sequencing Identifies Homozygous Mutation in TTI2 in a Child with Primary Microcephaly: a Case Report

Vincent Picher-Martel,Yvan Labrie,Serge Rivest,Baiba Lace,Nicolas Chrestian

BMC Neurology（2020）

Cited 9|Views22
Key words
TTI2,Microcephaly,Whole-exome sequencing,Case report
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