Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case report

Overview of attention for article published in BMC Pediatrics, September 2022

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Frameshift Mutation in LIS1 Gene is a Probable Cause of LIS

Physician's Weekly, 20 Oct 2022

Disorders of neuronal migration during embryogenesis lead to lissencephaly (LIS), a cortical deformity defined by a smooth or…

Lissencephaly: LIS1 Gene Frameshift Mutation

Physician's Weekly, 23 Sep 2022

Defective neuronal migration during embryogenesis results in the cortical deformity known as lissencephaly (LIS), characterized…

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