APA (7th ed.) Citation

Qarnain, Z., Khan, F., Akbar, F., & Kirmani, S. Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report). Wiley.

Chicago Style (17th ed.) Citation

Qarnain, Zul, Fatima Khan, Fizza Akbar, and Salman Kirmani. Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report). Wiley.

MLA (9th ed.) Citation

Qarnain, Zul, et al. Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report). Wiley.