Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report)

<div>Pedigree of the patient showing consanguinity in the parents (drawn using online tool; progeny genetics) (<a href="https://pedigree.progenygenetics.com/">https://pedigree.progenygenetics.com/</a>).</div>

Case Reports in Genetics

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Figure 2: Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report) 

Figure 2 | Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report) 